NDC 69367-192 - Phenazopyridine Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 69367-192
- Manufacturer
- NuCare Pharmaceuticals,Inc.
- Effective date
- 2023-12-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PHENAZOPYRIDINE HYDROCHLORIDE TABLETS, USP | NuCare Pharmaceuticals,Inc. | 2023-12-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenazopyridine Hydrochloride - DirectRx | DirectRx | 2023-11-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Phenazopyridine Hydrochloride - Proficient Rx LP | Proficient Rx LP | 2023-10-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69367-192-01 | EA - Each | 69367-192 | 43339bc3-d9d6-4899-82ae-3c5e23163257 | 1 | 2023-06-06 |