Phenazopyridine Hydrochloride
- Product NDC
- 71335-9712
- 11-digit product format
- 713359712
- Labeler code
- 71335
- Product ID
- 71335-9712_6d85dcea-2791-4542-bd15-e44edee59924
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-02-01
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0EWG668W17 | PHENAZOPYRIDINE HYDROCHLORIDE | 136-40-3 | PHENAZOPYRIDINE HYDROCHLORIDE |
| K2J09EMJ52 | PHENAZOPYRIDINE | 94-78-0 | Phenazopyridine |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-9712-1 | 71335971201 | 20 TABLET in 1 BOTTLE (71335-9712-1) | 20 tablet | 2024-12-12 | No | No | Historical |
| 71335-9712-2 | 71335971202 | 12 TABLET in 1 BOTTLE (71335-9712-2) | 12 tablet | 2024-12-12 | No | No | Historical |
| 71335-9712-3 | 71335971203 | 9 TABLET in 1 BOTTLE (71335-9712-3) | 9 tablet | 2024-12-12 | No | No | Historical |
| 71335-9712-4 | 71335971204 | 10 TABLET in 1 BOTTLE (71335-9712-4) | 10 tablet | 2023-06-12 | No | No | Historical |
| 71335-9712-5 | 71335971205 | 15 TABLET in 1 BOTTLE (71335-9712-5) | 15 tablet | 2023-05-08 | No | No | Historical |
| 71335-9712-6 | 71335971206 | 100 TABLET in 1 BOTTLE (71335-9712-6) | 100 tablet | 2024-12-12 | No | No | Historical |
| 71335-9712-7 | 71335971207 | 6 TABLET in 1 BOTTLE (71335-9712-7) | 6 tablet | 2024-12-12 | No | No | Historical |
| 71335-9712-8 | 71335971208 | 21 TABLET in 1 BOTTLE (71335-9712-8) | 21 tablet | 2024-12-12 | No | No | Historical |
| 71335-9712-9 | 71335971209 | 30 TABLET in 1 BOTTLE (71335-9712-9) | 30 tablet | 2024-12-12 | No | No | Historical |