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Tamsulosin Hydrochloride
Tamsulosin Hydrochloride - 62756-160-13 - (Tamsulosin Hydrochloride)
Drug Information of Tamsulosin Hydrochloride
| Product NDC: | 62756-160 |
| 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: | 62756-160 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090931 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100715 |
Package Information of Tamsulosin Hydrochloride
| Package NDC: | 62756-160-13 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (62756-160-13) |
NDC Information of Tamsulosin Hydrochloride
| NDC Code | 62756-160-13 |
| Proprietary Name | Tamsulosin Hydrochloride |
| Package Description | 500 CAPSULE in 1 BOTTLE (62756-160-13) |
| Product NDC | 62756-160 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tamsulosin Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100715 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | TAMSULOSIN HYDROCHLORIDE |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
