Vexia Maximum Strength Urinary Pain Relief
- Product NDC
- 10956-703
- 11-digit product format
- 109560703
- Labeler code
- 10956
- Product ID
- 10956-703_117fb757-2c46-4923-855d-4438e1976e49
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PHENAZOPYRIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Reese Pharmaceutical Co
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-05-24
- 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
- Vexia 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 |
|---|
| 10956-703-24 | Vexia Maximum Strength Urinary Pain Relief | 24 in 1 BLISTER PACK | TABLET | 24 | | 4 |
| 10956-703-24 | Vexia Maximum Strength 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 |
|---|
| 10956-703 | VEXIA MAXIMUM STRENGTH URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [REESE PHARMACEUTICAL CO] | 3 | Current NDC, 2 package rows | 20241220_5fbc47d2-cecd-4187-9bcc-51b1d0b7695d.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 |
|---|
| 10956-703-24 | 10956070324 | 1 BLISTER PACK in 1 CARTON (10956-703-24) / 24 TABLET in 1 BLISTER PACK | 1 blister pack | 2023-05-24 | No | No | Current |