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Propranolol Hydrochloride - 49349-190-02 - (Propranolol Hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 49349-190
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol Hydrochloride
Active Ingredient(s): 40    mg/1 & nbsp;   Propranolol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Propranolol Hydrochloride

Product NDC: 49349-190
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070177
Marketing Category: ANDA
Start Marketing Date: 20110419

Package Information of Propranolol Hydrochloride

Package NDC: 49349-190-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-190-02)

NDC Information of Propranolol Hydrochloride

NDC Code 49349-190-02
Proprietary Name Propranolol Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-190-02)
Product NDC 49349-190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110419
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


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