Phenazopyridine Hydrochloride
- Product NDC
- 67296-1231
- 11-digit product format
- 672961231
- Labeler code
- 67296
- Product ID
- 67296-1231_b34bb752-5b63-2c75-e053-2a95a90a23e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-02-01
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1231-6 | Phenazopyridine Hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1231 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20201105_b34bc5f6-0bbb-73fc-e053-2995a90a2552.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 |
|---|
| 67296-1231-6 | 67296123106 | 6 TABLET in 1 BOTTLE (67296-1231-6) | 6 tablet | 2011-02-01 | 0000-00-00 | No | No | Current |