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Tamsulosin Hydrochloride - 62756-160-13 - (Tamsulosin Hydrochloride)

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Drug Information of Tamsulosin Hydrochloride

Product NDC: 62756-160
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: 62756-160
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090931
Marketing Category: ANDA
Start Marketing Date: 20100715

Package Information of Tamsulosin Hydrochloride

Package NDC: 62756-160-13
Package Description: 500 CAPSULE in 1 BOTTLE (62756-160-13)

NDC Information of Tamsulosin Hydrochloride

NDC Code 62756-160-13
Proprietary Name Tamsulosin Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE (62756-160-13)
Product NDC 62756-160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamsulosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100715
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
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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