Active Ingredient: PHENAZOPYRIDINE HYDROCHLORIDE; SULFAMETHOXAZOLE
Proprietary Name: AZO GANTANOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG;500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N013294
Product Number: 001
Approval Date: Sep 10, 1987
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information