Fexofenadine Hydrochloride
- Product NDC
- 68210-4090
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- SPIRIT PHARMACEUTICALS LLC
- Application
- ANDA204507
- Marketing category
- ANDA
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68210-4090-1 | 100 TABLET, FILM COATED in 1 PACKAGE (68210-4090-1) | 20200702 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 5307b7ef-0c22-4aae-a2f6-033d31032f55 | Fexofenadine Hydrochloride Tablets, 180 mg | SPIRIT PHARMACEUTICALS LLC | 2024-12-13 | HUMAN OTC DRUG LABEL | 7 |