Fexofenadine HCL
- Product NDC
- 68071-4846
- 11-digit product format
- 680714846
- Labeler code
- 68071
- Product ID
- 68071-4846_bb8fff22-c6c7-4620-e053-2995a90ae117
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2016-08-19
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4846-9 | 68071484609 | 90 TABLET in 1 BOTTLE (68071-4846-9) | 90 tablet | 2019-04-15 | 0000-00-00 | No | No | Current |