Brevibloc - 10019-055-61 - (Esmolol Hydrochloride)

Alphabetical Index


Drug Information of Brevibloc

Product NDC: 10019-055
Proprietary Name: Brevibloc
Non Proprietary Name: Esmolol Hydrochloride
Active Ingredient(s): 10    mg/mL & nbsp;   Esmolol Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Brevibloc

Product NDC: 10019-055
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019386
Marketing Category: NDA
Start Marketing Date: 19861231

Package Information of Brevibloc

Package NDC: 10019-055-61
Package Description: 250 mL in 1 BAG (10019-055-61)

NDC Information of Brevibloc

NDC Code 10019-055-61
Proprietary Name Brevibloc
Package Description 250 mL in 1 BAG (10019-055-61)
Product NDC 10019-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Esmolol Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19861231
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name ESMOLOL HYDROCHLORIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Brevibloc


General Information