Childrens Fexofenadine Hydrochloride
- Product NDC
- 51672-2121
- 11-digit product format
- 516722121
- Labeler code
- 51672
- Product ID
- 51672-2121_d43ceeee-a210-45ca-a204-57c465c4e15c
- 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 |
|---|
| 51672-2121-1 | 51672212101 | 1 BOTTLE in 1 CARTON (51672-2121-1) > 240 mL in 1 BOTTLE | 1 bottle | 2017-11-09 | 0000-00-00 | No | No | Current |
| 51672-2121-4 | 51672212104 | 1 BOTTLE in 1 CARTON (51672-2121-4) > 60 mL in 1 BOTTLE | 1 bottle | 2017-11-09 | 0000-00-00 | No | No | Current |
| 51672-2121-8 | 51672212108 | 1 BOTTLE in 1 CARTON (51672-2121-8) > 120 mL in 1 BOTTLE | 1 bottle | 2017-11-09 | 0000-00-00 | No | No | Current |