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Phenazopyridine HCl - 52959-122-06 - (Phenazopyridine HCl)

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Drug Information of Phenazopyridine HCl

Product NDC: 52959-122
Proprietary Name: Phenazopyridine HCl
Non Proprietary Name: Phenazopyridine HCl
Active Ingredient(s): 200    mg/1 & nbsp;   Phenazopyridine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phenazopyridine HCl

Product NDC: 52959-122
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100910

Package Information of Phenazopyridine HCl

Package NDC: 52959-122-06
Package Description: 6 TABLET in 1 BOTTLE (52959-122-06)

NDC Information of Phenazopyridine HCl

NDC Code 52959-122-06
Proprietary Name Phenazopyridine HCl
Package Description 6 TABLET in 1 BOTTLE (52959-122-06)
Product NDC 52959-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenazopyridine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100910
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name H.J. Harkins Company, Inc.
Substance Name PHENAZOPYRIDINE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Phenazopyridine HCl


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