Allergy Relief
- Product NDC
- 54257-702
- 11-digit product format
- 542570702
- Labeler code
- 54257
- Product ID
- 54257-702_cf6e9191-0aff-f46f-e053-2995a90ad791
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FEXOFENADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Magno-Humphries, Inc.
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2020-01-24
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 54257-702-02 | 54257070202 | 100 TABLET in 1 BOTTLE (54257-702-02) | 100 tablet | 2020-01-24 | 0000-00-00 | No | No | Current |