Phenazopyridine Hydrochloride
- Product NDC
- 67296-1212
- 11-digit product format
- 672961212
- Labeler code
- 67296
- Product ID
- 67296-1212_d61018ec-f0b5-36df-e053-2995a90a0b29
- 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
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 67296-1212-6 | Phenazopyridine Hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1212 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20240716_b34bb613-9ae8-1c5f-e053-2995a90aae6a.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 |
|---|
| 67296-1212-6 | 67296121206 | 6 TABLET in 1 BOTTLE (67296-1212-6) | 6 tablet | 2011-02-01 | 0000-00-00 | No | No | Current |