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Tamsulosin Hydrochloride - 68788-0816-0 - (Tamsulosin Hydrochloride)

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Drug Information of Tamsulosin Hydrochloride

Product NDC: 68788-0816
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: 68788-0816
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078938
Marketing Category: ANDA
Start Marketing Date: 20101007

Package Information of Tamsulosin Hydrochloride

Package NDC: 68788-0816-0
Package Description: 100 CAPSULE in 1 BOTTLE (68788-0816-0)

NDC Information of Tamsulosin Hydrochloride

NDC Code 68788-0816-0
Proprietary Name Tamsulosin Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (68788-0816-0)
Product NDC 68788-0816
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamsulosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101007
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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


General Information