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Midazolam Hydrochloride - 10019-028-05 - (Midazolam Hydrochloride)

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Drug Information of Midazolam Hydrochloride

Product NDC: 10019-028
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: 10019-028
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075243
Marketing Category: ANDA
Start Marketing Date: 20100304

Package Information of Midazolam Hydrochloride

Package NDC: 10019-028-05
Package Description: 10 VIAL, MULTI-DOSE in 1 PACKAGE (10019-028-05) > 5 mL in 1 VIAL, MULTI-DOSE (10019-028-37)

NDC Information of Midazolam Hydrochloride

NDC Code 10019-028-05
Proprietary Name Midazolam Hydrochloride
Package Description 10 VIAL, MULTI-DOSE in 1 PACKAGE (10019-028-05) > 5 mL in 1 VIAL, MULTI-DOSE (10019-028-37)
Product NDC 10019-028
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midazolam Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100304
Marketing Category Name ANDA
Labeler Name Baxter Healthcare Corporation
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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