Urinary Pain Relief
- Product NDC
- 73581-909
- Requested package NDC
- 73581-909-72
- 11-digit product format
- 735810909
- Labeler code
- 73581
- Product ID
- 73581-909_f20534c0-4cd1-31f7-e053-2995a90a6879
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- YYBA CORP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-09-10
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73581-909-12 | Urinary Pain Relief | 120 in 1 BOTTLE | TABLET | 120 | | 7 |
| 73581-909-36 | Urinary Pain Relief | 36 in 1 BOTTLE | TABLET | 36 | | 7 |
| 73581-909-72 | Urinary Pain Relief | 72 in 1 BOTTLE | TABLET | 72 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73581-909 | URINARY PAIN RELIEF (PHENAZOPYRIDINE HYDROCHLORIDE) TABLET [YYBA CORP] | 4 | Legacy NDC, 3 package rows | 20250117_ad034f45-2852-f3c9-e053-2a95a90a38cb.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 |
|---|
| 73581-909-72 | 73581090972 | 72 TABLET in 1 BOTTLE (73581-909-72) | 72 tablet | 2020-09-10 | 0000-00-00 | No | No | Current |