Inderal - 24090-470-88 - (propranolol hydrochloride)

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Drug Information of Inderal

Product NDC: 24090-470
Proprietary Name: Inderal
Non Proprietary Name: propranolol hydrochloride
Active Ingredient(s): 60    mg/1 & nbsp;   propranolol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Inderal

Product NDC: 24090-470
Labeler Name: Akrimax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018553
Marketing Category: NDA
Start Marketing Date: 19830419

Package Information of Inderal

Package NDC: 24090-470-88
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24090-470-88)

NDC Information of Inderal

NDC Code 24090-470-88
Proprietary Name Inderal
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24090-470-88)
Product NDC 24090-470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propranolol hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19830419
Marketing Category Name NDA
Labeler Name Akrimax Pharmaceuticals, LLC
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Inderal


General Information