Childrens Fexofenadine Hydrochloride
- Product NDC
- 51672-2119
- 11-digit product format
- 516722119
- Labeler code
- 51672
- Product ID
- 51672-2119_2d6e0c2a-2637-4953-815d-3ffc22fbf9c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA208123
- Marketing category
- ANDA
- Marketing start
- 2017-11-09
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 30 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 51672-2119-1 | 51672211901 | 1 BOTTLE in 1 CARTON (51672-2119-1) > 240 mL in 1 BOTTLE | 1 bottle | 2017-11-09 | 0000-00-00 | No | No | Current |
| 51672-2119-4 | 51672211904 | 1 BOTTLE in 1 CARTON (51672-2119-4) > 60 mL in 1 BOTTLE | 1 bottle | 2017-11-09 | 0000-00-00 | No | No | Current |
| 51672-2119-8 | 51672211908 | 1 BOTTLE in 1 CARTON (51672-2119-8) > 120 mL in 1 BOTTLE | 1 bottle | 2017-11-09 | 0000-00-00 | No | No | Current |