Fexofenadine
- Product NDC
- 72189-305
- 11-digit product format
- 721890305
- Labeler code
- 72189
- Product ID
- 72189-305_d35a5ce4-cd84-5b1f-e053-2995a90a24db
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRx
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2021-12-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-305-30 | 72189030530 | 30 TABLET in 1 BOTTLE (72189-305-30) | 30 tablet | 2021-12-17 | 0000-00-00 | No | No | Current |