"70512-002-10" National Drug Code (NDC)

NDC Code	70512-002-10
Package Description	100 mg in 1 BOTTLE (70512-002-10)
Product NDC	70512-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenazopyridine
Non-Proprietary Name	Phenazopyridine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20180219
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	SOLA Pharmaceuticals
Substance Name	PHENAZOPYRIDINE HYDROCHLORIDE
Strength	100
Strength Unit	mg/mg