Flomax - 54868-4356-0 - (tamsulosin hydrochloride)

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Drug Information of Flomax

Product NDC: 54868-4356
Proprietary Name: Flomax
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 Flomax

Product NDC: 54868-4356
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020579
Marketing Category: NDA
Start Marketing Date: 20010828

Package Information of Flomax

Package NDC: 54868-4356-0
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-4356-0)

NDC Information of Flomax

NDC Code 54868-4356-0
Proprietary Name Flomax
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (54868-4356-0)
Product NDC 54868-4356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tamsulosin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20010828
Marketing Category Name NDA
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 Flomax


General Information