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tamsulosin hydrochloride - 43063-264-01 - (tamsulosin hydrochloride)

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Drug Information of tamsulosin hydrochloride

Product NDC: 43063-264
Proprietary Name: tamsulosin hydrochloride
Non Proprietary Name: tamsulosin hydrochloride
Active Ingredient(s): .4    mg/1 & nbsp;   tamsulosin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of tamsulosin hydrochloride

Product NDC: 43063-264
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078801
Marketing Category: ANDA
Start Marketing Date: 20100427

Package Information of tamsulosin hydrochloride

Package NDC: 43063-264-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (43063-264-01)

NDC Information of tamsulosin hydrochloride

NDC Code 43063-264-01
Proprietary Name tamsulosin hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (43063-264-01)
Product NDC 43063-264
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tamsulosin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100427
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name TAMSULOSIN HYDROCHLORIDE
Strength Number .4
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of tamsulosin hydrochloride


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