| 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) |
| 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 NDC: | 52389-241-12 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (52389-241-12) > 12 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-02) |
| NDC Code | 52389-241-12 |
| Proprietary Name | Uricalm |
| Package Description | 1 BLISTER PACK in 1 CARTON (52389-241-12) > 12 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-02) |
| 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 |