FLOMAX - 16590-489-30 - (TAMSULOSIN HYDROCHLORIDE)

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Drug Information of FLOMAX

Product NDC: 16590-489
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: 16590-489
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020579
Marketing Category: NDA
Start Marketing Date: 19970912

Package Information of FLOMAX

Package NDC: 16590-489-30
Package Description: 30 CAPSULE in 1 BOTTLE (16590-489-30)

NDC Information of FLOMAX

NDC Code 16590-489-30
Proprietary Name FLOMAX
Package Description 30 CAPSULE in 1 BOTTLE (16590-489-30)
Product NDC 16590-489
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TAMSULOSIN HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970912
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
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