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Terazosin hydrochloride
Terazosin hydrochloride - 0093-4338-10 - (Terazosin hydrochloride)
Drug Information of Terazosin hydrochloride
| Product NDC: | 0093-4338 |
| Proprietary Name: | Terazosin hydrochloride |
| Non Proprietary Name: | Terazosin hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Terazosin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terazosin hydrochloride
| Product NDC: | 0093-4338 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075614 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090908 |
Package Information of Terazosin hydrochloride
| Package NDC: | 0093-4338-10 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (0093-4338-10) |
NDC Information of Terazosin hydrochloride
| NDC Code | 0093-4338-10 |
| Proprietary Name | Terazosin hydrochloride |
| Package Description | 1000 CAPSULE in 1 BOTTLE (0093-4338-10) |
| Product NDC | 0093-4338 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terazosin hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090908 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | TERAZOSIN HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
