Fexofenadine hydrochloride
- Product NDC
- 68788-6848
- 11-digit product format
- 687886848
- Labeler code
- 68788
- Product ID
- 68788-6848_e483f90b-9ebc-4c2e-b2e9-73f81a60fe92
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202039
- Marketing category
- ANDA
- Marketing start
- 2016-12-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6848-1 | 68788684801 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-6848-1) | 2016-12-05 | 0000-00-00 | No | No | Current |
| 68788-6848-3 | 68788684803 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-6848-3) | 2016-12-05 | 0000-00-00 | No | No | Current |
| 68788-6848-6 | 68788684806 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-6848-6) | 2016-12-05 | 0000-00-00 | No | No | Current |
| 68788-6848-9 | 68788684809 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-6848-9) | 2016-12-05 | 0000-00-00 | No | No | Current |