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Propranolol Hydrochloride - 49884-330-10 - (Propranolol)

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Drug Information of Propranolol Hydrochloride

Product NDC: 49884-330
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol
Active Ingredient(s): 160    mg/1 & nbsp;   Propranolol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Propranolol Hydrochloride

Product NDC: 49884-330
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078065
Marketing Category: ANDA
Start Marketing Date: 20070126

Package Information of Propranolol Hydrochloride

Package NDC: 49884-330-10
Package Description: 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-330-10)

NDC Information of Propranolol Hydrochloride

NDC Code 49884-330-10
Proprietary Name Propranolol Hydrochloride
Package Description 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-330-10)
Product NDC 49884-330
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070126
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, Inc.
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 160
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


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