Phenazopyridine Hydrochloride
- Product NDC
- 68788-9501
- 11-digit product format
- 687889501
- Labeler code
- 68788
- Product ID
- 68788-9501_e6490bcd-a712-49f3-b5d6-adf1326d620c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2013-12-03
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68788-9501-1 | Phenazopyridine Hydrochloride | 10 in 1 BOTTLE | TABLET | 10 | | 4 |
| 68788-9501-2 | Phenazopyridine Hydrochloride | 20 in 1 BOTTLE | TABLET | 20 | | 4 |
| 68788-9501-3 | Phenazopyridine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 68788-9501-5 | Phenazopyridine Hydrochloride | 15 in 1 BOTTLE | TABLET | 15 | | 4 |
| 68788-9501-6 | Phenazopyridine Hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 4 |
| 68788-9501-9 | Phenazopyridine Hydrochloride | 9 in 1 BOTTLE | TABLET | 9 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| PHENAZOPYRIDINE HYDROCHLORIDE | ACTIVE INGREDIENT | 0EWG668W17 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| PHENAZOPYRIDINE | ACTIVE MOIETY | K2J09EMJ52 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| CARNAUBA WAX | INACTIVE INGREDIENT | R12CBM0EIZ | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-9501 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [PREFERRED PHARMACEUTICALS, INC.] | 4 | Legacy NDC, 6 package rows | 20171206_480ee010-26f9-479c-b472-91fed589c622.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68788-9501-1 | 68788950101 | 10 in 1 BOTTLE | Historical |
| 68788-9501-2 | 68788950102 | 20 in 1 BOTTLE | Historical |
| 68788-9501-3 | 68788950103 | 30 in 1 BOTTLE | Historical |
| 68788-9501-5 | 68788950105 | 15 in 1 BOTTLE | Historical |
| 68788-9501-6 | 68788950106 | 6 in 1 BOTTLE | Historical |
| 68788-9501-9 | 68788950109 | 9 in 1 BOTTLE | Historical |