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MIDAZOLAM Hydrochloride - 0409-2307-21 - (MIDAZOLAM HYDROCHLORIDE)

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Drug Information of MIDAZOLAM Hydrochloride

Product NDC: 0409-2307
Proprietary Name: MIDAZOLAM Hydrochloride
Non Proprietary Name: MIDAZOLAM HYDROCHLORIDE
Active Ingredient(s): 5    mg/mL & nbsp;   MIDAZOLAM HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MIDAZOLAM Hydrochloride

Product NDC: 0409-2307
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075856
Marketing Category: ANDA
Start Marketing Date: 20020613

Package Information of MIDAZOLAM Hydrochloride

Package NDC: 0409-2307-21
Package Description: 1 BLISTER PACK in 1 CARTON (0409-2307-21) > 10 SYRINGE in 1 BLISTER PACK > 1 mL in 1 SYRINGE

NDC Information of MIDAZOLAM Hydrochloride

NDC Code 0409-2307-21
Proprietary Name MIDAZOLAM Hydrochloride
Package Description 1 BLISTER PACK in 1 CARTON (0409-2307-21) > 10 SYRINGE in 1 BLISTER PACK > 1 mL in 1 SYRINGE
Product NDC 0409-2307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDAZOLAM HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20020613
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of MIDAZOLAM Hydrochloride


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