Fexofenadine hydrochloride
- Product NDC
- 71610-292
- 11-digit product format
- 716100292
- Labeler code
- 71610
- Product ID
- 71610-292_1554fdc4-77b0-4483-9cfb-59c004344ff6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA202039
- Marketing category
- ANDA
- Marketing start
- 2015-01-15
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71610-292 | FEXOFENADINE HYDROCHLORIDE TABLET, FILM COATED [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 1 | Legacy NDC | 20190610_b95d8c23-b4dd-4a53-bffd-ed6bc394060a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71610-292-30 | 71610029230 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-292-30) | 2019-06-06 | 0000-00-00 | No | No | Current |