Fexofenadine Hydrochloride
- Product NDC
- 51079-548
- 11-digit product format
- 510790548
- Labeler code
- 51079
- Product ID
- 51079-548_d1f32dc7-8a7d-e0a5-e053-2995a90a8963
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA077081
- Marketing category
- ANDA
- Marketing start
- 2011-09-27
- Marketing end
- 2022-02-28
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51079-548-20 | 51079054820 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-548-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-548-01) | 100 blister pack | 2011-09-27 | 0000-00-00 | No | No | Current |