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tamsulosin hydrochloride
tamsulosin hydrochloride - 0781-2076-10 - (tamsulosin hydrochloride)
Drug Information of tamsulosin hydrochloride
| Product NDC: | 0781-2076 |
| 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: | 0781-2076 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078015 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100427 |
Package Information of tamsulosin hydrochloride
| Package NDC: | 0781-2076-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (0781-2076-10) |
NDC Information of tamsulosin hydrochloride
| NDC Code | 0781-2076-10 |
| Proprietary Name | tamsulosin hydrochloride |
| Package Description | 1000 CAPSULE in 1 BOTTLE (0781-2076-10) |
| Product NDC | 0781-2076 |
| 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 | Sandoz Inc |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
