AZO - 49973-244-24 - (Urinary Pain Relief)

Alphabetical Index


Drug Information of AZO

Product NDC: 49973-244
Proprietary Name: AZO
Non Proprietary Name: Urinary Pain Relief
Active Ingredient(s): 97.5    mg/1 & nbsp;   Urinary Pain Relief
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of AZO

Product NDC: 49973-244
Labeler Name: i-Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120518

Package Information of AZO

Package NDC: 49973-244-24
Package Description: 12 BLISTER PACK in 1 BOX (49973-244-24) > 2 TABLET in 1 BLISTER PACK

NDC Information of AZO

NDC Code 49973-244-24
Proprietary Name AZO
Package Description 12 BLISTER PACK in 1 BOX (49973-244-24) > 2 TABLET in 1 BLISTER PACK
Product NDC 49973-244
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Urinary Pain Relief
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120518
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name i-Health, Inc.
Substance Name PHENAZOPYRIDINE HYDROCHLORIDE
Strength Number 97.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of AZO


General Information