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FLOMAX
FLOMAX - 16590-489-60 - (TAMSULOSIN HYDROCHLORIDE)
Drug Information of FLOMAX
| Product NDC: | 16590-489 |
| Proprietary Name: | FLOMAX |
| 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 FLOMAX
| Product NDC: | 16590-489 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020579 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970912 |
Package Information of FLOMAX
| Package NDC: | 16590-489-60 |
| Package Description: | 60 CAPSULE in 1 BOTTLE (16590-489-60) |
NDC Information of FLOMAX
| NDC Code | 16590-489-60 |
| Proprietary Name | FLOMAX |
| Package Description | 60 CAPSULE in 1 BOTTLE (16590-489-60) |
| Product NDC | 16590-489 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TAMSULOSIN HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19970912 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
