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Tamsulosin Hydrochloride - 51079-294-56 - (tamsulosin hydrochloride)

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Drug Information of Tamsulosin Hydrochloride

Product NDC: 51079-294
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: 51079-294
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090408
Marketing Category: ANDA
Start Marketing Date: 20121228

Package Information of Tamsulosin Hydrochloride

Package NDC: 51079-294-56
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-294-56) > 30 CAPSULE in 1 BLISTER PACK (51079-294-30)

NDC Information of Tamsulosin Hydrochloride

NDC Code 51079-294-56
Proprietary Name Tamsulosin Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-294-56) > 30 CAPSULE in 1 BLISTER PACK (51079-294-30)
Product NDC 51079-294
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name tamsulosin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121228
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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


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