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Flomax
Flomax - 49349-258-02 - (Flomax)
Drug Information of Flomax
| Product NDC: | 49349-258 |
| Proprietary Name: | Flomax |
| Non Proprietary Name: | Flomax |
| Active Ingredient(s): | .4 mg/1 & nbsp; Flomax |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flomax
| Product NDC: | 49349-258 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020579 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110330 |
Package Information of Flomax
| Package NDC: | 49349-258-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (49349-258-02) |
NDC Information of Flomax
| NDC Code | 49349-258-02 |
| Proprietary Name | Flomax |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (49349-258-02) |
| Product NDC | 49349-258 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flomax |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110330 |
| Marketing Category Name | NDA |
| 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] |
