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6505-01-362-7422

20 Products

PROSCAR TABLETS

FINASTERIDE TABLETS,USP

NSN, MFG P/N

6505013627422

NSN

6505-01-362-7422

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PROSCAR TABLETS

FINASTERIDE TABLETS,USP

NSN, MFG P/N

6505013627422

NSN

6505-01-362-7422

MFG

MERCK SHARP & DOHME CORP. DBA MERCK DIV US HUMAN HEALTH

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: FINASTERIDE TABLETS 5MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: 5 MG FINASTERIDE; USE FOR BENIGN PROSTATIC HYPERPLASIA
THERAPEUTIC EQUIVALENT: PROSE BY MERCK-SHARP AND DOHME

92-0933

ANTIDOTE TREATMENT

NSN, MFG P/N

6505013627427

NSN

6505-01-362-7427

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92-0933

ANTIDOTE TREATMENT

NSN, MFG P/N

6505013627427

NSN

6505-01-362-7427

MFG

DEFENSE MEDICAL STANDARDIZATION BOARD

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: AUTOINJECTOR, DUAL-CHAMBER: CONTAINING 2 MG OF ATROPINE INJECTION PER 0.7 ML, 2 ML OF PRALIODOXIME CHLORIDE INJECTION, 300 MG PER ML, AND ONE 21 GAGE STERILE NEEDLE; FOR INTRAMUSCULAR USE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIDOTE TREATMENT NERVE AGENT AUTO INJECTOR DUAL-CHAMBER

ATNAA

ANTIDOTE TREATMENT

NSN, MFG P/N

6505013627427

NSN

6505-01-362-7427

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ATNAA

ANTIDOTE TREATMENT

NSN, MFG P/N

6505013627427

NSN

6505-01-362-7427

MFG

MERIDIAN MEDICAL TECHNOLOGIES INC.

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: AUTOINJECTOR, DUAL-CHAMBER: CONTAINING 2 MG OF ATROPINE INJECTION PER 0.7 ML, 2 ML OF PRALIODOXIME CHLORIDE INJECTION, 300 MG PER ML, AND ONE 21 GAGE STERILE NEEDLE; FOR INTRAMUSCULAR USE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIDOTE TREATMENT NERVE AGENT AUTO INJECTOR DUAL-CHAMBER

NDC11704-0777-01

ANTIDOTE TREATMENT

NSN, MFG P/N

6505013627427

NSN

6505-01-362-7427

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NDC11704-0777-01

ANTIDOTE TREATMENT

NSN, MFG P/N

6505013627427

NSN

6505-01-362-7427

MFG

MERIDIAN MEDICAL TECHNOLOGIES INC.

Description

GENERAL CHARACTERISTICS ITEM DESCRIPTION: AUTOINJECTOR, DUAL-CHAMBER: CONTAINING 2 MG OF ATROPINE INJECTION PER 0.7 ML, 2 ML OF PRALIODOXIME CHLORIDE INJECTION, 300 MG PER ML, AND ONE 21 GAGE STERILE NEEDLE; FOR INTRAMUSCULAR USE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ANTIDOTE TREATMENT NERVE AGENT AUTO INJECTOR DUAL-CHAMBER

DRP 4/8 IND/H MAD

SODA LIME,NF

NSN, MFG P/N

6505013628311

NSN

6505-01-362-8311

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DRP 4/8 IND/H MAD

SODA LIME,NF

NSN, MFG P/N

6505013628311

NSN

6505-01-362-8311

MFG

DIVERS SUPPLY INC.

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODASORB
III PROTECTIVE STORAGE FEATURE: CORROSIVE AND POISONOUS
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.500 POUNDS OR 1.130 KILOGRAMS
PRIMARY CONTAINER TYPE: CARTRIDGE
SPECIAL FEATURES: GRANULAR SIZE BETWEEN 4 AND 8 MESH; W/INDICATOR; DISPOSABLE PLASTIC CARTRIDGE
TOTAL PRIMARY CONTAINER QUANTITY: 12

SODASORB PRE PAK

SODA LIME,NF

NSN, MFG P/N

6505013628311

NSN

6505-01-362-8311

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SODASORB PRE PAK

SODA LIME,NF

NSN, MFG P/N

6505013628311

NSN

6505-01-362-8311

MFG

GRACE W R AND CO DEWEY AND ALMY CHEMICAL DIV

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODASORB
III PROTECTIVE STORAGE FEATURE: CORROSIVE AND POISONOUS
III SUPPLEMENTARY FEATURES: D-DAY ITEM FOR DOD
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 2.500 POUNDS OR 1.130 KILOGRAMS
PRIMARY CONTAINER TYPE: CARTRIDGE
SPECIAL FEATURES: GRANULAR SIZE BETWEEN 4 AND 8 MESH; W/INDICATOR; DISPOSABLE PLASTIC CARTRIDGE
TOTAL PRIMARY CONTAINER QUANTITY: 12

COLYTE

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

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COLYTE

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

MFG

SCHWARZ PHARMA INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.530 GRAMS SODIUM CHLORIDE ACTIVE INGREDIENT AND 2.820 GRAMS POTASSIUM CHLORIDE ACTIVE INGREDIENT AND 6.360 GRAMS SODIUM BICARBONATE ACTIVE INGREDIENT AND 21.500 GRAMS SODIUM SULFATE, ANHYDROUS ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POLYETHYLENE GLYCOL AND ELECTROLYTES FOR ORAL SOLUTION 18OZ BT 12S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 510.300 GRAMS OR 18.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: CONTAINS 227.10 GRAMS POLYETHYLENE GLYCOL 3350 AND 1.83 GRAMS FLAVOR INGREDIENT
TOTAL PRIMARY CONTAINER QUANTITY: 12

COLYTE-FLAVORED

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

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COLYTE-FLAVORED

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

MFG

SCHWARZ PHARMA INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.530 GRAMS SODIUM CHLORIDE ACTIVE INGREDIENT AND 2.820 GRAMS POTASSIUM CHLORIDE ACTIVE INGREDIENT AND 6.360 GRAMS SODIUM BICARBONATE ACTIVE INGREDIENT AND 21.500 GRAMS SODIUM SULFATE, ANHYDROUS ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POLYETHYLENE GLYCOL AND ELECTROLYTES FOR ORAL SOLUTION 18OZ BT 12S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 510.300 GRAMS OR 18.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: CONTAINS 227.10 GRAMS POLYETHYLENE GLYCOL 3350 AND 1.83 GRAMS FLAVOR INGREDIENT
TOTAL PRIMARY CONTAINER QUANTITY: 12

NDC00021-4403-13

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

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NDC00021-4403-13

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

MFG

SCHWARZ PHARMA INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.530 GRAMS SODIUM CHLORIDE ACTIVE INGREDIENT AND 2.820 GRAMS POTASSIUM CHLORIDE ACTIVE INGREDIENT AND 6.360 GRAMS SODIUM BICARBONATE ACTIVE INGREDIENT AND 21.500 GRAMS SODIUM SULFATE, ANHYDROUS ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POLYETHYLENE GLYCOL AND ELECTROLYTES FOR ORAL SOLUTION 18OZ BT 12S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 510.300 GRAMS OR 18.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: CONTAINS 227.10 GRAMS POLYETHYLENE GLYCOL 3350 AND 1.83 GRAMS FLAVOR INGREDIENT
TOTAL PRIMARY CONTAINER QUANTITY: 12

NDC00091-4403-13

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

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NDC00091-4403-13

PEG 3350 AND ELECTROLYTES FOR ORAL SOLUTION,USP

NSN, MFG P/N

6505013628312

NSN

6505-01-362-8312

MFG

SCHWARZ PHARMA INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 5.530 GRAMS SODIUM CHLORIDE ACTIVE INGREDIENT AND 2.820 GRAMS POTASSIUM CHLORIDE ACTIVE INGREDIENT AND 6.360 GRAMS SODIUM BICARBONATE ACTIVE INGREDIENT AND 21.500 GRAMS SODIUM SULFATE, ANHYDROUS ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: POLYETHYLENE GLYCOL AND ELECTROLYTES FOR ORAL SOLUTION 18OZ BT 12S
PHYSICAL FORM: POWDER
PRIMARY CONTAINER CONTENT QUANTITY: 510.300 GRAMS OR 18.000 OUNCES
PRIMARY CONTAINER TYPE: BOTTLE
SPECIAL FEATURES: CONTAINS 227.10 GRAMS POLYETHYLENE GLYCOL 3350 AND 1.83 GRAMS FLAVOR INGREDIENT
TOTAL PRIMARY CONTAINER QUANTITY: 12

INFED

IRON DEXTRAN INJECTION,USP

NSN, MFG P/N

6505013628314

NSN

6505-01-362-8314

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INFED

IRON DEXTRAN INJECTION,USP

NSN, MFG P/N

6505013628314

NSN

6505-01-362-8314

MFG

SCHEIN HENRY INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS IRON EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAVENOUS OR INTRAMUSCULAR
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IRON DEXTRAN INJECTION USP 2ML AMPUL 10S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00364-3012-47

IRON DEXTRAN INJECTION,USP

NSN, MFG P/N

6505013628314

NSN

6505-01-362-8314

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NDC00364-3012-47

IRON DEXTRAN INJECTION,USP

NSN, MFG P/N

6505013628314

NSN

6505-01-362-8314

MFG

SCHEIN HENRY INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS IRON EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAVENOUS OR INTRAMUSCULAR
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IRON DEXTRAN INJECTION USP 2ML AMPUL 10S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC52544-0931-02

IRON DEXTRAN INJECTION,USP

NSN, MFG P/N

6505013628314

NSN

6505-01-362-8314

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NDC52544-0931-02

IRON DEXTRAN INJECTION,USP

NSN, MFG P/N

6505013628314

NSN

6505-01-362-8314

MFG

WATSON LABS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 50.000 MILLIGRAMS IRON EQUIVALENT PER MILLILITER
ADMINISTRATION: INTRAVENOUS OR INTRAMUSCULAR
III PART NAME ASSIGNED BY CONTROLLING AGENCY: IRON DEXTRAN INJECTION USP 2ML AMPUL 10S
III PROTECTIVE STORAGE FEATURE: SUBJECT TO DAMAGE BY FREEZING
PHARMACEUTICAL VEHICLE TYPE: AQUEOUS
PRIMARY CONTAINER CONTENT QUANTITY: 2.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
TOTAL PRIMARY CONTAINER QUANTITY: 10

NDC00074-6660-75

SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505013629903

NSN

6505-01-362-9903

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NDC00074-6660-75

SODIUM CHLORIDE INJECTION,USP

NSN, MFG P/N

6505013629903

NSN

6505-01-362-9903

MFG

HOSPIRA INC.

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 2.500 MILLIEQUIVALENTS SODIUM CHLORIDE INJECTION PER MILLILITER
III PART NAME ASSIGNED BY CONTROLLING AGENCY: SODIUM CHLORIDE INJECTION USP 40ML VIAL 100S
III SUPPLEMENTARY FEATURES: 100 MEQ PER 40 ML
PRIMARY CONTAINER CONTENT QUANTITY: 40.000 MILLILITERS
PRIMARY CONTAINER TYPE: VIAL
SECONDARY CONTAINER TYPE: BOX
SPECIAL FEATURES: 25 TO A BOX; SOLD IN MULTIPLES OF 4
TOTAL PRIMARY CONTAINER QUANTITY: 25

CARDIZEM CD

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630019

NSN

6505-01-363-0019

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CARDIZEM CD

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630019

NSN

6505-01-363-0019

MFG

SANOFI-AVENTIS U.S. INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 180.000 MILLIGRAMS DILTIAZEM HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: PELLET
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 5000.000
CAPSULE TYPE: SOFT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DILTIAZEM EXTENDED-RELEASE CAPSULES USP 180MG 5000S DRUM
PRIMARY CONTAINER TYPE: DRUM
THERAPEUTIC EQUIVALENT: MARION MERRELL DOW

NDC00088-1796-90

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630019

NSN

6505-01-363-0019

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NDC00088-1796-90

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630019

NSN

6505-01-363-0019

MFG

SANOFI-AVENTIS U.S. INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 180.000 MILLIGRAMS DILTIAZEM HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: PELLET
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 5000.000
CAPSULE TYPE: SOFT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DILTIAZEM EXTENDED-RELEASE CAPSULES USP 180MG 5000S DRUM
PRIMARY CONTAINER TYPE: DRUM
THERAPEUTIC EQUIVALENT: MARION MERRELL DOW

CARDIZEM CD

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630020

NSN

6505-01-363-0020

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CARDIZEM CD

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630020

NSN

6505-01-363-0020

MFG

SANOFI-AVENTIS U.S. INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 240.000 MILLIGRAMS DILTIAZEM HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: PELLET
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 5000.000
CAPSULE TYPE: SOFT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DILTIAZEM EXTENDED-RELEASE CAPSULES USP 240MG 5000S DRUM
PRIMARY CONTAINER TYPE: PACKAGE

NDC00088-1797-90

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630020

NSN

6505-01-363-0020

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NDC00088-1797-90

DILTIAZEM EXTENDED-RELEASE CAPSULES,USP

NSN, MFG P/N

6505013630020

NSN

6505-01-363-0020

MFG

SANOFI-AVENTIS U.S. INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 240.000 MILLIGRAMS DILTIAZEM HYDROCHLORIDE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
CAPSULE CONTENT FORM: PELLET
CAPSULE PRIMARY CONTAINER CONTENT QUANTITY: 5000.000
CAPSULE TYPE: SOFT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: DILTIAZEM EXTENDED-RELEASE CAPSULES USP 240MG 5000S DRUM
PRIMARY CONTAINER TYPE: PACKAGE

CEPACOL

CETYLPYRIDINIUM CHLORIDE LOZENGES,USP

NSN, MFG P/N

6505013630558

NSN

6505-01-363-0558

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CEPACOL

CETYLPYRIDINIUM CHLORIDE LOZENGES,USP

NSN, MFG P/N

6505013630558

NSN

6505-01-363-0558

MFG

COMBE INCORPORATED

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: CETYLPYRIDINIUM CHLORIDE LOZENGES USP 432S PG
PRIMARY CONTAINER CONTENT QUANTITY: 9.000 LOZENGES
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 2 STRIP
PRIMARY CONTAINER TYPE: STRIP
SECONDARY CONTAINER TYPE: BOX
SPECIAL FEATURES: 18 LOZENGES PER BOX; 24 BOXES PER PG
TOTAL PRIMARY CONTAINER QUANTITY: 24

CEPACOL LOZENGES

CETYLPYRIDINIUM CHLORIDE LOZENGES,USP

NSN, MFG P/N

6505013630558

NSN

6505-01-363-0558

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CEPACOL LOZENGES

CETYLPYRIDINIUM CHLORIDE LOZENGES,USP

NSN, MFG P/N

6505013630558

NSN

6505-01-363-0558

MFG

COMBE INCORPORATED

Description

III PART NAME ASSIGNED BY CONTROLLING AGENCY: CETYLPYRIDINIUM CHLORIDE LOZENGES USP 432S PG
PRIMARY CONTAINER CONTENT QUANTITY: 9.000 LOZENGES
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 2 STRIP
PRIMARY CONTAINER TYPE: STRIP
SECONDARY CONTAINER TYPE: BOX
SPECIAL FEATURES: 18 LOZENGES PER BOX; 24 BOXES PER PG
TOTAL PRIMARY CONTAINER QUANTITY: 24