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Metronidazole - 0409-7811-37 - (METRONIDAZOLE)

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Drug Information of Metronidazole

Product NDC: 0409-7811
Proprietary Name: Metronidazole
Non Proprietary Name: METRONIDAZOLE
Active Ingredient(s): 500    mg/100mL & nbsp;   METRONIDAZOLE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Metronidazole

Product NDC: 0409-7811
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018890
Marketing Category: NDA
Start Marketing Date: 19831118

Package Information of Metronidazole

Package NDC: 0409-7811-37
Package Description: 20 POUCH in 1 CASE (0409-7811-37) > 4 BAG in 1 POUCH > 100 mL in 1 BAG

NDC Information of Metronidazole

NDC Code 0409-7811-37
Proprietary Name Metronidazole
Package Description 20 POUCH in 1 CASE (0409-7811-37) > 4 BAG in 1 POUCH > 100 mL in 1 BAG
Product NDC 0409-7811
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METRONIDAZOLE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19831118
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name METRONIDAZOLE
Strength Number 500
Strength Unit mg/100mL
Pharmaceutical Classes Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient]

Complete Information of Metronidazole


General Information