Phenazopyridine Hydrochloride
- Product NDC
- 71186-004
- 11-digit product format
- 711860004
- Labeler code
- 71186
- Product ID
- 71186-004_f82a4c45-dc39-4423-b66b-073113d0ae51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Vilvet Pharmaceuticals Inc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-05-01
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 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 |
|---|
| 71186-004-25 | Phenazopyridine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71186-004 | PHENAZOPYRIDINE HYDROCHLORIDE TABLET, FILM COATED [VILVET PHARMACEUTICALS INC] | 5 | Legacy NDC, 1 package rows | 20190308_2b92007f-74d3-45a6-9d2f-3ea052b7c008.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 71186-004-25 | 71186000425 | 100 in 1 BOTTLE | Historical |