Uricalm - 52389-241-36 - (Phenazopyridine Hydochloride)

Alphabetical Index


Drug Information of Uricalm

Product NDC: 52389-241
Proprietary Name: Uricalm
Non Proprietary Name: Phenazopyridine Hydochloride
Active Ingredient(s): 99.5    mg/1 & nbsp;   Phenazopyridine Hydochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Uricalm

Product NDC: 52389-241
Labeler Name: Alva-Amco Pharmacal Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20080429

Package Information of Uricalm

Package NDC: 52389-241-36
Package Description: 1 BLISTER PACK in 1 CARTON (52389-241-36) > 36 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-03)

NDC Information of Uricalm

NDC Code 52389-241-36
Proprietary Name Uricalm
Package Description 1 BLISTER PACK in 1 CARTON (52389-241-36) > 36 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-03)
Product NDC 52389-241
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Phenazopyridine Hydochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080429
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Alva-Amco Pharmacal Companies, Inc.
Substance Name PHENAZOPYRIDINE HYDROCHLORIDE
Strength Number 99.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Uricalm


General Information