Phenazopyridine Hydrochloride
- Product NDC
- 50436-4388
- 11-digit product format
- 504364388
- Labeler code
- 50436
- Product ID
- 50436-4388_8158963c-7e9a-4d61-8ee4-0bf99d496486
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- 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
- 2020-12-31
- 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 |
|---|
| 50436-4388-1 | Phenazopyridine Hydrochloride | 10 in 1 BOTTLE | TABLET | 10 | | 8 |
| 50436-4388-2 | Phenazopyridine Hydrochloride | 8 in 1 BOTTLE | TABLET | 8 | | 8 |
| 50436-4388-9 | Phenazopyridine Hydrochloride | 9 in 1 BOTTLE | TABLET | 9 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-4388 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [UNIT DOSE SERVICES] | 8 | Legacy NDC, 3 package rows | 20190509_849fa5d5-fc5e-4225-a4fc-e8346ef89369.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-4388-1 | 50436438801 | 10 in 1 BOTTLE | Historical |
| 50436-4388-2 | 50436438802 | 8 in 1 BOTTLE | Historical |
| 50436-4388-9 | 50436438809 | 9 in 1 BOTTLE | Historical |