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Tamsulosin Hydrochloride - 54868-4437-2 - (TAMSULOSIN HYDROCHLORIDE)

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Drug Information of Tamsulosin Hydrochloride

Product NDC: 54868-4437
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: 54868-4437
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090377
Marketing Category: ANDA
Start Marketing Date: 20100310

Package Information of Tamsulosin Hydrochloride

Package NDC: 54868-4437-2
Package Description: 30 CAPSULE in 1 BOTTLE (54868-4437-2)

NDC Information of Tamsulosin Hydrochloride

NDC Code 54868-4437-2
Proprietary Name Tamsulosin Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (54868-4437-2)
Product NDC 54868-4437
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TAMSULOSIN HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100310
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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