Phenazopyridine Hydrochloride
- Product NDC
- 71335-2014
- 11-digit product format
- 713352014
- Labeler code
- 71335
- Product ID
- 71335-2014_0344418a-5429-4835-9f2f-0a42638d51bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-08-23
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 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 | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0EWG668W17 |
| Rxcui | 1094107 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2014-1 | Phenazopyridine Hydrochloride | 20 in 1 BOTTLE | TABLET | 20 | | 101 |
| 71335-2014-2 | Phenazopyridine Hydrochloride | 12 in 1 BOTTLE | TABLET | 12 | | 101 |
| 71335-2014-3 | Phenazopyridine Hydrochloride | 9 in 1 BOTTLE | TABLET | 9 | | 101 |
| 71335-2014-4 | Phenazopyridine Hydrochloride | 10 in 1 BOTTLE | TABLET | 10 | | 101 |
| 71335-2014-5 | Phenazopyridine Hydrochloride | 15 in 1 BOTTLE | TABLET | 15 | | 101 |
| 71335-2014-6 | Phenazopyridine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 101 |
| 71335-2014-7 | Phenazopyridine Hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 101 |
| 71335-2014-8 | Phenazopyridine Hydrochloride | 21 in 1 BOTTLE | TABLET | 21 | | 101 |
| 71335-2014-9 | Phenazopyridine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2014 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, Legacy NDC, 9 package rows | 20231110_5cb06cfe-9d4e-4900-9989-6445ea55542e.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 |
|---|
| 71335-2014-1 | 71335201401 | 20 TABLET in 1 BOTTLE (71335-2014-1) | 20 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-2 | 71335201402 | 12 TABLET in 1 BOTTLE (71335-2014-2) | 12 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-3 | 71335201403 | 9 TABLET in 1 BOTTLE (71335-2014-3) | 9 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-4 | 71335201404 | 10 TABLET in 1 BOTTLE (71335-2014-4) | 10 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-5 | 71335201405 | 15 TABLET in 1 BOTTLE (71335-2014-5) | 15 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-6 | 71335201406 | 100 TABLET in 1 BOTTLE (71335-2014-6) | 100 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-7 | 71335201407 | 6 TABLET in 1 BOTTLE (71335-2014-7) | 6 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-8 | 71335201408 | 21 TABLET in 1 BOTTLE (71335-2014-8) | 21 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |
| 71335-2014-9 | 71335201409 | 30 TABLET in 1 BOTTLE (71335-2014-9) | 30 tablet | 2022-02-10 | 0000-00-00 | No | No | Current |