Minipress - 0069-4310-71 - (PRAZOSIN HYDROCHLORIDE)

Alphabetical Index


Drug Information of Minipress

Product NDC: 0069-4310
Proprietary Name: Minipress
Non Proprietary Name: PRAZOSIN HYDROCHLORIDE
Active Ingredient(s): 1    mg/1 & nbsp;   PRAZOSIN HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Minipress

Product NDC: 0069-4310
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017442
Marketing Category: NDA
Start Marketing Date: 19940510

Package Information of Minipress

Package NDC: 0069-4310-71
Package Description: 250 CAPSULE in 1 BOTTLE (0069-4310-71)

NDC Information of Minipress

NDC Code 0069-4310-71
Proprietary Name Minipress
Package Description 250 CAPSULE in 1 BOTTLE (0069-4310-71)
Product NDC 0069-4310
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRAZOSIN HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19940510
Marketing Category Name NDA
Labeler Name Pfizer Laboratories Div Pfizer Inc
Substance Name PRAZOSIN HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Minipress


General Information