Phenazopyridine Hydrochloride
- Product NDC
- 68151-1992
- 11-digit product format
- 681511992
- Labeler code
- 68151
- Product ID
- 68151-1992_5ef9ac99-fd51-4f37-8c2e-1875a1c0a52f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-08-23
- 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 |
|---|
| 68151-1992-0 | Phenazopyridine Hydrochloride | 1 in 1 PACKAGE | TABLET | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-1992 | PHENAZOPYRIDINE HYDROCHLORIDE (PHENAZOPYRIDINE) TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20140707_43c1b32c-23dc-45c7-afc1-b61599eb7258.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-1992-0 | 68151199200 | 1 in 1 PACKAGE | Historical |