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TAMSULOSIN HYDROCHLORIDE
TAMSULOSIN HYDROCHLORIDE - 64679-516-02 - (TAMSULOSIN HYDROCHLORIDE)
Drug Information of TAMSULOSIN HYDROCHLORIDE
| Product NDC: | 64679-516 |
| 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: | 64679-516 |
| Labeler Name: | WOCKHARDT USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078938 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100427 |
Package Information of TAMSULOSIN HYDROCHLORIDE
| Package NDC: | 64679-516-02 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (64679-516-02) |
NDC Information of TAMSULOSIN HYDROCHLORIDE
| NDC Code | 64679-516-02 |
| Proprietary Name | TAMSULOSIN HYDROCHLORIDE |
| Package Description | 100 CAPSULE in 1 BOTTLE (64679-516-02) |
| Product NDC | 64679-516 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TAMSULOSIN HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100427 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT USA LLC |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
