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Prazosin Hydrochloride
Prazosin Hydrochloride - 51079-631-20 - (prazosin hydrochloride)
Drug Information of Prazosin Hydrochloride
| Product NDC: | 51079-631 |
| 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: | 51079-631 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072575 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110128 |
Package Information of Prazosin Hydrochloride
| Package NDC: | 51079-631-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-631-20) > 1 CAPSULE in 1 BLISTER PACK (51079-631-01) |
NDC Information of Prazosin Hydrochloride
| NDC Code | 51079-631-20 |
| Proprietary Name | Prazosin Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-631-20) > 1 CAPSULE in 1 BLISTER PACK (51079-631-01) |
| Product NDC | 51079-631 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prazosin hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110128 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | PRAZOSIN HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |
