Phenazopyridine Hydrochloride
- Product NDC
- 72162-2540
- 11-digit product format
- 721622540
- Labeler code
- 72162
- Product ID
- 72162-2540_06b34ac0-9193-4ecc-934a-729ac7e7b7e7
- 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
- 200 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 |
|---|
| 72162-2540-1 | 72162254001 | 100 TABLET in 1 BOTTLE (72162-2540-1) | 100 tablet | 2025-09-19 | No | No | Historical |