Preferred Urinary Pain Relief
- Product NDC
- 10956-551
- 11-digit product format
- 109560551
- Labeler code
- 10956
- Product ID
- 10956-551_5ee931f8-50ce-49e3-8ae8-8ca96ef3dfb6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PHENAZOPYRIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Reese Pharmaceutical Co
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2013-07-01
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 95 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
- Preferred Urinary Pain Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | 95 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0EWG668W17 |
| Rxcui | 1094126 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10956-551-30 | Preferred Urinary Pain Relief | 30 in 1 BLISTER PACK | TABLET | 30 | | 4 |
| 10956-551-30 | Preferred Urinary Pain Relief | 1 in 1 CARTON | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10956-551 | PREFERRED URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [REESE PHARMACEUTICAL CO] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241220_668f59c9-e543-49fc-96f5-a8077f760529.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10956-551-30 | 10956055130 | 1 BLISTER PACK in 1 CARTON (10956-551-30) / 30 TABLET in 1 BLISTER PACK | 1 blister pack | 2016-07-27 | 0000-00-00 | No | No | Current |