Flomax - 55154-0407-0 - (tamsulosin hydrochloride)

Alphabetical Index


Drug Information of Flomax

Product NDC: 55154-0407
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: 55154-0407
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020579
Marketing Category: NDA
Start Marketing Date: 19970912

Package Information of Flomax

Package NDC: 55154-0407-0
Package Description: 10 POUCH in 1 BAG (55154-0407-0) > 1 CAPSULE in 1 POUCH

NDC Information of Flomax

NDC Code 55154-0407-0
Proprietary Name Flomax
Package Description 10 POUCH in 1 BAG (55154-0407-0) > 1 CAPSULE in 1 POUCH
Product NDC 55154-0407
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 Cardinal Health
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