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6505-01-096-2734

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NDC50111-0471-01

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505010962734

NSN

6505-01-096-2734

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NDC50111-0471-01

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505010962734

NSN

6505-01-096-2734

MFG

PLIVA INC .

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 80.000 MILLIGRAMS PROPRANOLOL HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PROPRANOLOL HYDROCHLORIDE TABLETS USP 80MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

PERCODAN

OXYCODONE AND ASPIRIN TABLETS,USP

NSN, MFG P/N

6505010958570

NSN

6505-01-095-8570

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PERCODAN

OXYCODONE AND ASPIRIN TABLETS,USP

NSN, MFG P/N

6505010958570

NSN

6505-01-095-8570

MFG

BRISTOL-MYERS SQUIBB PHARMA COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 325.000 MILLIGRAMS ASPIRIN ACTIVE INGREDIENT AND 4.500 MILLIGRAMS OXYCODONE HYDROCHLORIDE ACTIVE INGREDIENT AND 0.380 MILLIGRAMS OXYCODONE TEREPHTHALATE ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 500.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

MYLANTA

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

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MYLANTA

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

MFG

MCNEIL CONSUMER PRODUCTS CO HOSPITAL REGIONAL OFFICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED PER MILLILITER AND 40.000 MILLIGRAMS MAGNESIUM HYDROXIDE PER MILLILITER AND 4.000 MILLIGRAMS DIMETHICONE PER MILLILITER
ADMINISTRATION: ORAL
FLAVOR: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ALUMINUM HYDROXIDE GEL MAGNESIUM HYDROXIDE & SIMETHICONE SUSPENSION 30ML 100S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,MCNEIL LABS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 10 CUPS,UNIT DOSE
PRIMARY CONTAINER TYPE: CUP,UNIT DOSE
SECONDARY CONTAINER TYPE: TRAY
TOTAL PRIMARY CONTAINER QUANTITY: 100
TOTAL SECONDARY CONTAINER QUANTITY: 10

MYLANTA SUSPENSION

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

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MYLANTA SUSPENSION

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

MFG

MCNEIL CONSUMER PRODUCTS CO HOSPITAL REGIONAL OFFICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED PER MILLILITER AND 40.000 MILLIGRAMS MAGNESIUM HYDROXIDE PER MILLILITER AND 4.000 MILLIGRAMS DIMETHICONE PER MILLILITER
ADMINISTRATION: ORAL
FLAVOR: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ALUMINUM HYDROXIDE GEL MAGNESIUM HYDROXIDE & SIMETHICONE SUSPENSION 30ML 100S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,MCNEIL LABS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 10 CUPS,UNIT DOSE
PRIMARY CONTAINER TYPE: CUP,UNIT DOSE
SECONDARY CONTAINER TYPE: TRAY
TOTAL PRIMARY CONTAINER QUANTITY: 100
TOTAL SECONDARY CONTAINER QUANTITY: 10

NDC00038-0610-23

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

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NDC00038-0610-23

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

MFG

ZENECA INC ZENECA PHARMACEUTICALS GROUP STUART PHARMACEUTICALS

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED PER MILLILITER AND 40.000 MILLIGRAMS MAGNESIUM HYDROXIDE PER MILLILITER AND 4.000 MILLIGRAMS DIMETHICONE PER MILLILITER
ADMINISTRATION: ORAL
FLAVOR: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ALUMINUM HYDROXIDE GEL MAGNESIUM HYDROXIDE & SIMETHICONE SUSPENSION 30ML 100S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,MCNEIL LABS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 10 CUPS,UNIT DOSE
PRIMARY CONTAINER TYPE: CUP,UNIT DOSE
SECONDARY CONTAINER TYPE: TRAY
TOTAL PRIMARY CONTAINER QUANTITY: 100
TOTAL SECONDARY CONTAINER QUANTITY: 10

NDC00045-0610-23

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

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NDC00045-0610-23

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

MFG

MCNEIL LAB INC MCNEIL PHARMACEUTICAL DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED PER MILLILITER AND 40.000 MILLIGRAMS MAGNESIUM HYDROXIDE PER MILLILITER AND 4.000 MILLIGRAMS DIMETHICONE PER MILLILITER
ADMINISTRATION: ORAL
FLAVOR: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ALUMINUM HYDROXIDE GEL MAGNESIUM HYDROXIDE & SIMETHICONE SUSPENSION 30ML 100S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,MCNEIL LABS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 10 CUPS,UNIT DOSE
PRIMARY CONTAINER TYPE: CUP,UNIT DOSE
SECONDARY CONTAINER TYPE: TRAY
TOTAL PRIMARY CONTAINER QUANTITY: 100
TOTAL SECONDARY CONTAINER QUANTITY: 10

NDC16837-0610-23

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

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NDC16837-0610-23

ALUMINA,MAGNESIA,AND SIMETHICONE ORAL SUSPENSION,USP

NSN, MFG P/N

6505010959185

NSN

6505-01-095-9185

MFG

MCNEIL CONSUMER PRODUCTS CO HOSPITAL REGIONAL OFFICE

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 40.000 MILLIGRAMS ALUMINUM HYDROXIDE GEL, DRIED PER MILLILITER AND 40.000 MILLIGRAMS MAGNESIUM HYDROXIDE PER MILLILITER AND 4.000 MILLIGRAMS DIMETHICONE PER MILLILITER
ADMINISTRATION: ORAL
FLAVOR: ANY ACCEPTABLE
III PART NAME ASSIGNED BY CONTROLLING AGENCY: ALUMINUM HYDROXIDE GEL MAGNESIUM HYDROXIDE & SIMETHICONE SUSPENSION 30ML 100S
III SUPPLEMENTARY FEATURES: MEDSEP ITEM FOR DOD,MCNEIL LABS
PRIMARY CONTAINER CONTENT QUANTITY: 30.000 MILLILITERS
PRIMARY CONTAINER QUANTITY PER SECONDARY CONTAINER: 10 CUPS,UNIT DOSE
PRIMARY CONTAINER TYPE: CUP,UNIT DOSE
SECONDARY CONTAINER TYPE: TRAY
TOTAL PRIMARY CONTAINER QUANTITY: 100
TOTAL SECONDARY CONTAINER QUANTITY: 10

14243

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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14243

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

LASIX

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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LASIX

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

HOECHST-ROUSSEL PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00039-0067-70

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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NDC00039-0067-70

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

HOECHST-ROUSSEL PHARMACEUTICALS INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00054-4297-31

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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NDC00054-4297-31

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

BOEHRINGER INGELHEIM ROXANE INC. DIV SUB OF BOEHRINGER INGELHEIM CORP

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00182-1170-10

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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NDC00182-1170-10

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

GOLDLINE LABORATORIES INC. DBA GOLDLINE LABORATORIES

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00364-0568-02

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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NDC00364-0568-02

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

SCHEIN HENRY INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00536-3840-10

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

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NDC00536-3840-10

FUROSEMIDE TABLETS,USP

NSN, MFG P/N

6505010960621

NSN

6505-01-096-0621

MFG

RUGBY GROUP INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 20.000 MILLIGRAMS FUROSEMIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: FUROSEMIDE TABLETS USP 20MG 1000S BT
PRIMARY CONTAINER CONTENT QUANTITY: 1000.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

ATIVAN

LORAZEPAM TABLETS,USP

NSN, MFG P/N

6505010960623

NSN

6505-01-096-0623

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ATIVAN

LORAZEPAM TABLETS,USP

NSN, MFG P/N

6505010960623

NSN

6505-01-096-0623

MFG

AMERICAN HOME PRODUCTS CORP WYETH-AYERST LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 MILLIGRAMS LORAZEPAM ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00008-0081-02

LORAZEPAM TABLETS,USP

NSN, MFG P/N

6505010960623

NSN

6505-01-096-0623

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NDC00008-0081-02

LORAZEPAM TABLETS,USP

NSN, MFG P/N

6505010960623

NSN

6505-01-096-0623

MFG

AMERICAN HOME PRODUCTS CORP WYETH-AYERST LABORATORIES DIV

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 MILLIGRAMS LORAZEPAM ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

NDC00536-3959-01

LORAZEPAM TABLETS,USP

NSN, MFG P/N

6505010960623

NSN

6505-01-096-0623

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NDC00536-3959-01

LORAZEPAM TABLETS,USP

NSN, MFG P/N

6505010960623

NSN

6505-01-096-0623

MFG

RUGBY GROUP INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 0.500 MILLIGRAMS LORAZEPAM ACTIVE INGREDIENT
ADMINISTRATION: ORAL
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE

08-8356-1

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505010960626

NSN

6505-01-096-0626

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08-8356-1

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505010960626

NSN

6505-01-096-0626

MFG

HERMES CONSOLIDATED INC. DBA WYOMING REFINING COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 3.500 MILLIEQUIVALENTS CALCIUM ION PER LITER AND 102.000 MILLIEQUIVALENTS CHLORIDE ION PER LITER AND 2.000 GRAMS DEXTROSE PER LITER AND 135.000 MILLIEQUIVALENTS SODIUM ION PER LITER AND 38.000 MILLIEQUIVALENTS ACETATE ION PER LITER AND 0.500
PRIMARY CONTAINER CONTENT QUANTITY: 3430.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC
SPECIAL FEATURES: STRENGTHS IN PAC AKJA ARE AFTER DILUTION OF 1 PART SOLUTION WITH 34 PARTS WATER
TOTAL PRIMARY CONTAINER QUANTITY: 4
~1: MILLIEQUIVALENTS MAGNESIUM ION PER LITER AND 1.000 MILLIEQUIVALENTS POTASSIUM ION PER LITER

ERI-LYTE

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505010960626

NSN

6505-01-096-0626

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ERI-LYTE

HEMODIALYSIS SOLUTION,CONCENTRATED

NSN, MFG P/N

6505010960626

NSN

6505-01-096-0626

MFG

HERMES CONSOLIDATED INC. DBA WYOMING REFINING COMPANY

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 3.500 MILLIEQUIVALENTS CALCIUM ION PER LITER AND 102.000 MILLIEQUIVALENTS CHLORIDE ION PER LITER AND 2.000 GRAMS DEXTROSE PER LITER AND 135.000 MILLIEQUIVALENTS SODIUM ION PER LITER AND 38.000 MILLIEQUIVALENTS ACETATE ION PER LITER AND 0.500
PRIMARY CONTAINER CONTENT QUANTITY: 3430.000 MILLILITERS
PRIMARY CONTAINER TYPE: BOTTLE, PLASTIC
SPECIAL FEATURES: STRENGTHS IN PAC AKJA ARE AFTER DILUTION OF 1 PART SOLUTION WITH 34 PARTS WATER
TOTAL PRIMARY CONTAINER QUANTITY: 4
~1: MILLIEQUIVALENTS MAGNESIUM ION PER LITER AND 1.000 MILLIEQUIVALENTS POTASSIUM ION PER LITER

NDC00536-4316-01

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505010962734

NSN

6505-01-096-2734

View More Info

NDC00536-4316-01

PROPRANOLOL HYDROCHLORIDE TABLETS,USP

NSN, MFG P/N

6505010962734

NSN

6505-01-096-2734

MFG

RUGBY GROUP INC

Description

ACTIVE MEDICAMENT MEDICINAL STRENGTH: 80.000 MILLIGRAMS PROPRANOLOL HYDROCHLORIDE ACTIVE INGREDIENT
III PART NAME ASSIGNED BY CONTROLLING AGENCY: PROPRANOLOL HYDROCHLORIDE TABLETS USP 80MG 100S BT
PRIMARY CONTAINER CONTENT QUANTITY: 100.000 TABLETS
PRIMARY CONTAINER TYPE: BOTTLE