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Terazosin Hydrochloride
Terazosin Hydrochloride - 35356-962-30 - (Terazosin Hydrochloride)
Drug Information of Terazosin Hydrochloride
| Product NDC: | 35356-962 |
| Proprietary Name: | Terazosin Hydrochloride |
| Non Proprietary Name: | Terazosin Hydrochloride |
| Active Ingredient(s): | 2 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: | 35356-962 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075317 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of Terazosin Hydrochloride
| Package NDC: | 35356-962-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (35356-962-30) |
NDC Information of Terazosin Hydrochloride
| NDC Code | 35356-962-30 |
| Proprietary Name | Terazosin Hydrochloride |
| Package Description | 30 CAPSULE in 1 BOTTLE (35356-962-30) |
| Product NDC | 35356-962 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terazosin Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | TERAZOSIN HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
