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PROPRANOLOL - 16590-808-60 - (PROPRANOLOL HYDROCHLORIDE)

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Drug Information of PROPRANOLOL

Product NDC: 16590-808
Proprietary Name: PROPRANOLOL
Non Proprietary Name: PROPRANOLOL HYDROCHLORIDE
Active Ingredient(s): 10    mg/1 & nbsp;   PROPRANOLOL HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of PROPRANOLOL

Product NDC: 16590-808
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070175
Marketing Category: ANDA
Start Marketing Date: 19860101

Package Information of PROPRANOLOL

Package NDC: 16590-808-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (16590-808-60)

NDC Information of PROPRANOLOL

NDC Code 16590-808-60
Proprietary Name PROPRANOLOL
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (16590-808-60)
Product NDC 16590-808
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PROPRANOLOL HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19860101
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of PROPRANOLOL


General Information