INNOPRAN - 0173-0791-01 - (propranolol hydrochloride)

Alphabetical Index


Drug Information of INNOPRAN

Product NDC: 0173-0791
Proprietary Name: INNOPRAN
Non Proprietary Name: propranolol hydrochloride
Active Ingredient(s): 120    mg/1 & nbsp;   propranolol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of INNOPRAN

Product NDC: 0173-0791
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021438
Marketing Category: NDA
Start Marketing Date: 20080328

Package Information of INNOPRAN

Package NDC: 0173-0791-01
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0173-0791-01)

NDC Information of INNOPRAN

NDC Code 0173-0791-01
Proprietary Name INNOPRAN
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0173-0791-01)
Product NDC 0173-0791
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propranolol hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080328
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of INNOPRAN


General Information