Maximum Strength Urinary Pain Relief
- Product NDC
- 80513-517
- 11-digit product format
- 805130517
- Labeler code
- 80513
- Product ID
- 80513-517_1b87f423-20e1-743e-e063-6294a90aaa03
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Advanced Rx LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2024-05-01
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 99.5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Maximum Strength Urinary Pain Relief
- Listing expiration
- 2026-12-31
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 |
|---|
| 80513-517-72 | Maximum Strength Urinary Pain Relief | 72 in 1 BOTTLE | TABLET | 72 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80513-517 | MAXIMUM STRENGTH URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [ADVANCED RX LLC] | 1 | Current NDC, 1 package rows | 20240625_a10464cf-36b2-460f-b31c-2e0edee3e4cf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 80513-517-72 | 80513051772 | 72 TABLET in 1 BOTTLE (80513-517-72) | 72 tablet | 2024-05-01 | No | No | Current |