Phenazopyridine Hydrochloride
- Product NDC
- 71335-2323
- 11-digit product format
- 713352323
- Labeler code
- 71335
- Product ID
- 71335-2323_f4ccf1f2-79d0-484a-802b-1ab625c1cb7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-10-19
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 71335-2323_f4ccf1f2-79d0-484a-802b-1ab625c1cb7e
- SPL ID
- f4ccf1f2-79d0-484a-802b-1ab625c1cb7e
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Phenazopyridine Hydrochloride
- Generic name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Marketing start
- 2023-10-19
- Marketing category
- UNAPPROVED DRUG OTHER
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | 100 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 0EWG668W17 |
| Rxcui | 1094107 |
| Spl Set Id | 25a1d5cf-7ede-4ece-8ec9-ccf979355d98 |
| Manufacturer Name | Bryant Ranch Prepack |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 71335-2323-1 | 20 TABLET in 1 BOTTLE (71335-2323-1) | 2024-01-04 | No |
| 71335-2323-2 | 12 TABLET in 1 BOTTLE (71335-2323-2) | 2024-01-04 | No |
| 71335-2323-3 | 9 TABLET in 1 BOTTLE (71335-2323-3) | 2024-01-04 | No |
| 71335-2323-4 | 10 TABLET in 1 BOTTLE (71335-2323-4) | 2024-01-04 | No |
| 71335-2323-5 | 15 TABLET in 1 BOTTLE (71335-2323-5) | 2024-01-04 | No |
| 71335-2323-6 | 100 TABLET in 1 BOTTLE (71335-2323-6) | 2024-01-04 | No |
| 71335-2323-7 | 6 TABLET in 1 BOTTLE (71335-2323-7) | 2024-01-04 | No |
| 71335-2323-8 | 21 TABLET in 1 BOTTLE (71335-2323-8) | 2024-01-04 | No |
| 71335-2323-9 | 30 TABLET in 1 BOTTLE (71335-2323-9) | 2024-01-04 | No |
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 |
|---|
| 71335-2323-1 | 71335232301 | 20 TABLET in 1 BOTTLE (71335-2323-1) | 20 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-2 | 71335232302 | 12 TABLET in 1 BOTTLE (71335-2323-2) | 12 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-3 | 71335232303 | 9 TABLET in 1 BOTTLE (71335-2323-3) | 9 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-4 | 71335232304 | 10 TABLET in 1 BOTTLE (71335-2323-4) | 10 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-5 | 71335232305 | 15 TABLET in 1 BOTTLE (71335-2323-5) | 15 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-6 | 71335232306 | 100 TABLET in 1 BOTTLE (71335-2323-6) | 100 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-7 | 71335232307 | 6 TABLET in 1 BOTTLE (71335-2323-7) | 6 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-8 | 71335232308 | 21 TABLET in 1 BOTTLE (71335-2323-8) | 21 tablet | 2024-01-04 | No | No | Historical |
| 71335-2323-9 | 71335232309 | 30 TABLET in 1 BOTTLE (71335-2323-9) | 30 tablet | 2024-01-04 | No | No | Historical |