| NDC Code | 70934-740-12 |
|---|
| Package Description | 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-740-12) |
|---|
| Product NDC | 70934-740 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phenazopyridine Hydrochloride |
|---|
| Non-Proprietary Name | Phenazopyridine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200526 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
|---|
| Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|