Phenazopyridine Hydrochloride
- Product NDC
- 68071-2583
- 11-digit product format
- 680712583
- Labeler code
- 68071
- Product ID
- 68071-2583_25a5b3ec-717d-4f5d-e063-6294a90ad965
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-02-01
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-2583-1 | Phenazopyridine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
| 68071-2583-3 | Phenazopyridine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
| 68071-2583-6 | Phenazopyridine Hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2583 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [NUCARE PHARMACEUTICALS,INC.] | 6 | Current NDC, Legacy NDC, 3 package rows | 20241031_d1f4ec5c-ca63-7ccd-e053-2a95a90a0db7.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 |
|---|
| 68071-2583-1 | 68071258301 | 100 TABLET in 1 BOTTLE (68071-2583-1) | 100 tablet | 2021-11-29 | 0000-00-00 | No | No | Current |
| 68071-2583-3 | 68071258303 | 30 TABLET in 1 BOTTLE (68071-2583-3) | 30 tablet | 2021-11-29 | | No | No | Historical |
| 68071-2583-6 | 68071258306 | 6 TABLET in 1 BOTTLE (68071-2583-6) | 6 tablet | 2024-10-29 | | No | No | Historical |