Home > National Drug Code (NDC) > Propranolol Hydrochloride

Propranolol Hydrochloride - 0228-2779-11 - (Propranolol Hydrochloride)

Alphabetical Index


Drug Information of Propranolol Hydrochloride

Product NDC: 0228-2779
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol Hydrochloride
Active Ingredient(s): 80    mg/1 & nbsp;   Propranolol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Propranolol Hydrochloride

Product NDC: 0228-2779
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078494
Marketing Category: ANDA
Start Marketing Date: 20070810

Package Information of Propranolol Hydrochloride

Package NDC: 0228-2779-11
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2779-11)

NDC Information of Propranolol Hydrochloride

NDC Code 0228-2779-11
Proprietary Name Propranolol Hydrochloride
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2779-11)
Product NDC 0228-2779
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070810
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


General Information