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Tamsulosin Hydrochloride
Tamsulosin Hydrochloride - 63739-567-10 - (Tamsulosin Hydrochloride)
Drug Information of Tamsulosin Hydrochloride
| Product NDC: | 63739-567 |
| 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: | 63739-567 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078225 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120809 |
Package Information of Tamsulosin Hydrochloride
| Package NDC: | 63739-567-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-567-10) > 10 CAPSULE in 1 BLISTER PACK |
NDC Information of Tamsulosin Hydrochloride
| NDC Code | 63739-567-10 |
| Proprietary Name | Tamsulosin Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-567-10) > 10 CAPSULE in 1 BLISTER PACK |
| Product NDC | 63739-567 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tamsulosin Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120809 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
