Fexofenadine hydrochloride
- Product NDC
- 70518-2971
- 11-digit product format
- 705182971
- Labeler code
- 70518
- Product ID
- 70518-2971_ed228e92-8f5a-7306-e053-2995a90adb7b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076502
- Marketing category
- ANDA
- Marketing start
- 2020-12-16
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2S068B75ZU | FEXOFENADINE HYDROCHLORIDE | 153439-40-8 | FEXOFENADINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2971-0 | 70518297100 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-2971-0) | 100 tablet | 2020-12-16 | 0000-00-00 | No | No | Current |
| 70518-2971-1 | 70518297101 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2971-1) | 30 tablet | 2022-04-27 | 0000-00-00 | No | No | Current |