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Tamsulosin Hydrochloride - 49349-401-24 - (Tamsulosin Hydrochloride)

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Drug Information of Tamsulosin Hydrochloride

Product NDC: 49349-401
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: 49349-401
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078938
Marketing Category: ANDA
Start Marketing Date: 20110720

Package Information of Tamsulosin Hydrochloride

Package NDC: 49349-401-24
Package Description: 200 CAPSULE in 1 CANISTER (49349-401-24)

NDC Information of Tamsulosin Hydrochloride

NDC Code 49349-401-24
Proprietary Name Tamsulosin Hydrochloride
Package Description 200 CAPSULE in 1 CANISTER (49349-401-24)
Product NDC 49349-401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamsulosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110720
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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