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Terazosin
Terazosin - 60505-0118-1 - (Terazosin)
Drug Information of Terazosin
| Product NDC: | 60505-0118 |
| Proprietary Name: | Terazosin |
| Non Proprietary Name: | Terazosin |
| Active Ingredient(s): | 10 mg/1 & nbsp; Terazosin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terazosin
| Product NDC: | 60505-0118 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075498 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010412 |
Package Information of Terazosin
| Package NDC: | 60505-0118-1 |
| Package Description: | 1000 CAPSULE in 1 BOTTLE (60505-0118-1) |
NDC Information of Terazosin
| NDC Code | 60505-0118-1 |
| Proprietary Name | Terazosin |
| Package Description | 1000 CAPSULE in 1 BOTTLE (60505-0118-1) |
| Product NDC | 60505-0118 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terazosin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20010412 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | TERAZOSIN HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
