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Midazolam Hydrochloride - 0409-2305-49 - (MIDAZOLAM HYDROCHLORIDE)

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Drug Information of Midazolam Hydrochloride

Product NDC: 0409-2305
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Midazolam Hydrochloride

Product NDC: 0409-2305
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075857
Marketing Category: ANDA
Start Marketing Date: 20020722

Package Information of Midazolam Hydrochloride

Package NDC: 0409-2305-49
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-2305-49) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Midazolam Hydrochloride

NDC Code 0409-2305-49
Proprietary Name Midazolam Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-2305-49) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-2305
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDAZOLAM HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20020722
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
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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