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Phenazopyridine Hydrochloride - 21695-301-16 - (Phenazopyridine)

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Drug Information of Phenazopyridine Hydrochloride

Product NDC: 21695-301
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: 21695-301
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110201

Package Information of Phenazopyridine Hydrochloride

Package NDC: 21695-301-16
Package Description: 16 TABLET in 1 BOTTLE (21695-301-16)

NDC Information of Phenazopyridine Hydrochloride

NDC Code 21695-301-16
Proprietary Name Phenazopyridine Hydrochloride
Package Description 16 TABLET in 1 BOTTLE (21695-301-16)
Product NDC 21695-301
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 Rebel Distributors Corp
Substance Name PHENAZOPYRIDINE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Phenazopyridine Hydrochloride


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