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InnoPran XL - 24090-451-85 - (propranolol hydrochloride)

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Drug Information of InnoPran XL

Product NDC: 24090-451
Proprietary Name: InnoPran XL
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 XL

Product NDC: 24090-451
Labeler Name: Akrimax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021438
Marketing Category: NDA
Start Marketing Date: 20130601

Package Information of InnoPran XL

Package NDC: 24090-451-85
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24090-451-85)

NDC Information of InnoPran XL

NDC Code 24090-451-85
Proprietary Name InnoPran XL
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (24090-451-85)
Product NDC 24090-451
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propranolol hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130601
Marketing Category Name NDA
Labeler Name Akrimax Pharmaceuticals, 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 XL


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