Phenazopyridine Hydrochloride
- Product NDC
- 10135-621
- 11-digit product format
- 101350621
- Labeler code
- 10135
- Product ID
- 10135-621_bb26518a-bd8f-31c3-e053-2a95a90ab405
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenazopyridine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals Inc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-10-01
- Marketing end
- 0000-00-00
- Substance
- PHENAZOPYRIDINE HYDROCHLORIDE
- Active strength
- 200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 10135-621-01 | 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 |
|---|
| 10135-621 | PHENAZOPYRIDINE HYDROCHLORIDE TABLET, FILM COATED [MARLEX PHARMACEUTICALS INC] | 5 | Legacy NDC, 1 package rows | 20210213_50182fc6-0d06-4095-be87-e9674daa6496.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10135-621-01 | 10135062101 | 100 TABLET, FILM COATED in 1 BOTTLE (10135-621-01) | 2016-10-01 | 0000-00-00 | No | No | Current |