Phenazopyridine Hydrochloride
- Product NDC
- 53217-178
- 11-digit product format
- 532170178
- Labeler code
- 53217
- Product ID
- 53217-178_e61daff9-c6e3-4251-87a5-8cf3baf678c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- 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
- 2019-12-31
- 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 |
|---|
| 53217-178-10 | Phenazopyridine Hydrochloride | 10 in 1 BOTTLE | TABLET | 10 | | 1 |
| 53217-178-12 | Phenazopyridine Hydrochloride | 12 in 1 BOTTLE | TABLET | 12 | | 1 |
| 53217-178-20 | Phenazopyridine Hydrochloride | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
| 53217-178-30 | Phenazopyridine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-178 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 4 package rows | 20170225_b4d22d69-b225-46b8-84a1-52321bb88804.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-178-10 | 53217017810 | 10 in 1 BOTTLE | Historical |
| 53217-178-12 | 53217017812 | 12 in 1 BOTTLE | Historical |
| 53217-178-20 | 53217017820 | 20 in 1 BOTTLE | Historical |
| 53217-178-30 | 53217017830 | 30 in 1 BOTTLE | Historical |