Home > National Drug Code (NDC) > Prazosin Hydrochloride

Prazosin Hydrochloride - 51079-631-20 - (prazosin hydrochloride)

Alphabetical Index


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]

Complete Information of Prazosin Hydrochloride


General Information