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Prazosin Hydrochloride
Prazosin Hydrochloride - 54868-1547-1 - (Prazosin Hydrochloride)
Drug Information of Prazosin Hydrochloride
| Product NDC: | 54868-1547 |
| Proprietary Name: | Prazosin Hydrochloride |
| Non Proprietary Name: | Prazosin Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Prazosin Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prazosin Hydrochloride
| Product NDC: | 54868-1547 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071995 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070222 |
Package Information of Prazosin Hydrochloride
| Package NDC: | 54868-1547-1 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (54868-1547-1) |
NDC Information of Prazosin Hydrochloride
| NDC Code | 54868-1547-1 |
| Proprietary Name | Prazosin Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (54868-1547-1) |
| Product NDC | 54868-1547 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prazosin Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070222 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | PRAZOSIN HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
