Home
>
National Drug Code (NDC)
>
Tamsulosin Hydrochloride
Tamsulosin Hydrochloride - 52125-017-02 - (Tamsulosin Hydrochloride)
Drug Information of Tamsulosin Hydrochloride
| Product NDC: | 52125-017 |
| 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: | 52125-017 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077630 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130227 |
Package Information of Tamsulosin Hydrochloride
| Package NDC: | 52125-017-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (52125-017-02) |
NDC Information of Tamsulosin Hydrochloride
| NDC Code | 52125-017-02 |
| Proprietary Name | Tamsulosin Hydrochloride |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (52125-017-02) |
| Product NDC | 52125-017 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tamsulosin Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130227 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
