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Phenazopyridine Hydrochloride - 63629-1595-2 - (Phenazopyridine)

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Drug Information of Phenazopyridine Hydrochloride

Product NDC: 63629-1595
Proprietary Name: Phenazopyridine Hydrochloride
Non Proprietary Name: Phenazopyridine
Active Ingredient(s): 200    mg/1 & nbsp;   Phenazopyridine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phenazopyridine Hydrochloride

Product NDC: 63629-1595
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110201

Package Information of Phenazopyridine Hydrochloride

Package NDC: 63629-1595-2
Package Description: 20 TABLET in 1 BOTTLE (63629-1595-2)

NDC Information of Phenazopyridine Hydrochloride

NDC Code 63629-1595-2
Proprietary Name Phenazopyridine Hydrochloride
Package Description 20 TABLET in 1 BOTTLE (63629-1595-2)
Product NDC 63629-1595
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenazopyridine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110201
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Bryant Ranch Prepack
Substance Name PHENAZOPYRIDINE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Phenazopyridine Hydrochloride


General Information