fexofenadine hcl
- Product NDC
- 51407-034
- 11-digit product format
- 514070034
- Labeler code
- 51407
- Product ID
- 51407-034_cecb8f12-d978-5acb-e053-2995a90a5176
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hcl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2015-09-16
- Marketing end
- 2022-07-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-034-01 | 51407003401 | 100 TABLET, FILM COATED in 1 BOTTLE (51407-034-01) | 2018-01-01 | 0000-00-00 | No | No | Current |
| 51407-034-05 | 51407003405 | 500 TABLET, FILM COATED in 1 BOTTLE (51407-034-05) | 2018-01-01 | 0000-00-00 | No | No | Current |