Diazepam - 0409-3213-12 - (DIAZEPAM)

Alphabetical Index


Drug Information of Diazepam

Product NDC: 0409-3213
Proprietary Name: Diazepam
Non Proprietary Name: DIAZEPAM
Active Ingredient(s): 5    mg/mL & nbsp;   DIAZEPAM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Diazepam

Product NDC: 0409-3213
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071583
Marketing Category: ANDA
Start Marketing Date: 19871013

Package Information of Diazepam

Package NDC: 0409-3213-12
Package Description: 10 VIAL, MULTI-DOSE in 1 BOX (0409-3213-12) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Diazepam

NDC Code 0409-3213-12
Proprietary Name Diazepam
Package Description 10 VIAL, MULTI-DOSE in 1 BOX (0409-3213-12) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-3213
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DIAZEPAM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19871013
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DIAZEPAM
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Diazepam


General Information