Phenazopyridine Hydrochloride
- Product NDC
- 75826-115
- 11-digit product format
- 758260115
- Labeler code
- 75826
- Product ID
- 75826-115_e0537551-5536-d23c-e053-2995a90af439
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Winder Laboratories, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-11-23
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenazopyridine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0EWG668W17 |
| Rxcui | 1094104, 1094107 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75826-115-10 | Phenazopyridine Hydrochloride | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75826-115 | PHENAZOPYRIDINE HYDROCHLORIDE TABLET [WINDER LABORATORIES, LLC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20220601_0a190e86-4074-4822-888e-4952281712ea.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 |
|---|
| 75826-115-10 | 75826011510 | 100 TABLET in 1 BOTTLE, PLASTIC (75826-115-10) | 100 tablet | 2015-11-23 | 0000-00-00 | No | No | Current |