Flomax - 63629-3384-4 - (tamsulosin hydrochloride)

Alphabetical Index


Drug Information of Flomax

Product NDC: 63629-3384
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: 63629-3384
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020579
Marketing Category: NDA
Start Marketing Date: 19970912

Package Information of Flomax

Package NDC: 63629-3384-4
Package Description: 180 CAPSULE in 1 BOTTLE (63629-3384-4)

NDC Information of Flomax

NDC Code 63629-3384-4
Proprietary Name Flomax
Package Description 180 CAPSULE in 1 BOTTLE (63629-3384-4)
Product NDC 63629-3384
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 Bryant Ranch Prepack
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