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Prazosin Hydrochloride - 43063-248-30 - (prazosin hydrochloride)

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Drug Information of Prazosin Hydrochloride

Product NDC: 43063-248
Proprietary Name: Prazosin Hydrochloride
Non Proprietary Name: prazosin hydrochloride
Active Ingredient(s): 5    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: 43063-248
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072575
Marketing Category: ANDA
Start Marketing Date: 20100210

Package Information of Prazosin Hydrochloride

Package NDC: 43063-248-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-248-30)

NDC Information of Prazosin Hydrochloride

NDC Code 43063-248-30
Proprietary Name Prazosin Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-248-30)
Product NDC 43063-248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prazosin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100210
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name PRAZOSIN HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Prazosin Hydrochloride


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