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Midazolam hydrochloride - 55648-762-04 - (Midazolam hydrochloride)

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Drug Information of Midazolam hydrochloride

Product NDC: 55648-762
Proprietary Name: Midazolam hydrochloride
Non Proprietary Name: Midazolam hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Midazolam hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Midazolam hydrochloride

Product NDC: 55648-762
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078141
Marketing Category: ANDA
Start Marketing Date: 20080530

Package Information of Midazolam hydrochloride

Package NDC: 55648-762-04
Package Description: 25 VIAL in 1 CARTON (55648-762-04) > 2 mL in 1 VIAL (55648-762-07)

NDC Information of Midazolam hydrochloride

NDC Code 55648-762-04
Proprietary Name Midazolam hydrochloride
Package Description 25 VIAL in 1 CARTON (55648-762-04) > 2 mL in 1 VIAL (55648-762-07)
Product NDC 55648-762
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midazolam hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080530
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam hydrochloride


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