Preferred Urinary Pain Relief
- Product NDC
- 68071-4417
- 11-digit product format
- 680714417
- Labeler code
- 68071
- Product ID
- 68071-4417_bb7c6fe8-93b0-a9b5-e053-2995a90aba81
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PHENAZOPYRIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2013-07-01
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 95 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4417-3 | 68071441703 | 30 TABLET in 1 BOX (68071-4417-3) | 30 tablet | 2018-05-04 | 0000-00-00 | No | No | Current |