Urinary Pain Relief
- Product NDC
- 73581-919
- 11-digit product format
- 735810919
- Labeler code
- 73581
- Product ID
- 73581-919_5137d15a-1390-d5f1-e063-6394a90aabfd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- YYBA CORP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-04-01
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 99.5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Urinary Pain Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | 99.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0EWG668W17 |
| Rxcui | 1094147 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73581-919-12 | Urinary Pain Relief | 120 in 1 BOTTLE | TABLET | 120 | | 1 |
| 73581-919-36 | Urinary Pain Relief | 36 in 1 BOTTLE | TABLET | 36 | | 1 |
| 73581-919-72 | Urinary Pain Relief | 72 in 1 BOTTLE | TABLET | 72 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73581-919-12 | 73581091912 | 120 TABLET in 1 BOTTLE (73581-919-12) | 120 tablet | 2026-04-01 | No | No | Historical |
| 73581-919-36 | 73581091936 | 36 TABLET in 1 BOTTLE (73581-919-36) | 36 tablet | 2026-04-01 | No | No | Historical |
| 73581-919-72 | 73581091972 | 72 TABLET in 1 BOTTLE (73581-919-72) | 72 tablet | 2026-04-01 | No | No | Historical |