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FDA Approval

Phenazopyridine Hydrochloride

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Effective Date
January 18, 2022
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Phenazopyridine(200 mg in 1 1)

Products2

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Phenazopyridine Hydrochloride

Product Details

NDC Product Code
73028-202
Route of Administration
ORAL
Effective Date
January 18, 2022
Code: 0EWG668W17Class: ACTIBQuantity: 200 mg in 1 1

Phenazopyridine Hydrochloride

Product Details

NDC Product Code
73028-201
Route of Administration
ORAL
Effective Date
January 18, 2022
Code: 0EWG668W17Class: ACTIBQuantity: 100 mg in 1 1
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