Phenazopyridine Hydrochloride
- Product NDC
- 82804-995
- 11-digit product format
- 828040995
- Labeler code
- 82804
- Product ID
- 82804-995_ac155091-ee07-46da-bb25-ff4cd4074610
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-10-19
- 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 |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-995-00 | 82804099500 | 100 TABLET in 1 BOTTLE (82804-995-00) | 100 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-06 | 82804099506 | 6 TABLET in 1 BOTTLE (82804-995-06) | 6 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-10 | 82804099510 | 10 TABLET in 1 BOTTLE (82804-995-10) | 10 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-12 | 82804099512 | 12 TABLET in 1 BOTTLE (82804-995-12) | 12 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-20 | 82804099520 | 20 TABLET in 1 BOTTLE (82804-995-20) | 20 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-24 | 82804099524 | 24 TABLET in 1 BOTTLE (82804-995-24) | 24 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-55 | 82804099555 | 500 TABLET in 1 BOTTLE (82804-995-55) | 500 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-90 | 82804099590 | 90 TABLET in 1 BOTTLE (82804-995-90) | 90 tablet | 2024-05-06 | No | No | Historical |
| 82804-995-96 | 82804099596 | 96 TABLET in 1 BOTTLE (82804-995-96) | 96 tablet | 2024-05-06 | No | No | Historical |