Fexofenadine HCl
- Product NDC
- 50090-2457
- 11-digit product format
- 500902457
- Labeler code
- 50090
- Product ID
- 50090-2457_5f2932b8-0d2d-4180-be30-d8c1f9952578
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2015-09-16
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2457-0 | Fexofenadine HCl | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 18 |
| 50090-2457-1 | Fexofenadine HCl | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2457 | FEXOFENADINE HCL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 18 | Legacy NDC, 2 package rows | 20200121_53beda1f-3aa1-4ba9-ae70-d69b6fbe4ebc.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 |
|---|
| 50090-2457-0 | 50090245700 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-2457-0) | 2016-08-24 | 0000-00-00 | No | No | Current |
| 50090-2457-1 | 50090245701 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-2457-1) | 2016-08-12 | 0000-00-00 | No | No | Current |