Allergy Relief
- Product NDC
- 63868-667
- 11-digit product format
- 638680667
- Labeler code
- 63868
- Product ID
- 63868-667_d010a735-1a1f-23fe-e053-2995a90abe0f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC.
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2018-09-01
- Marketing end
- 2023-02-28
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 63868-667-15 | 63868066715 | 3 BLISTER PACK in 1 CARTON (63868-667-15) > 5 TABLET in 1 BLISTER PACK | 3 blister pack | 2018-09-01 | 0000-00-00 | No | No | Current |
| 63868-667-30 | 63868066730 | 1 BOTTLE, PLASTIC in 1 CARTON (63868-667-30) > 30 TABLET in 1 BOTTLE, PLASTIC | | 2018-09-01 | 0000-00-00 | No | No | Current |
| 63868-667-45 | 63868066745 | 1 BOTTLE, PLASTIC in 1 CARTON (63868-667-45) > 45 TABLET in 1 BOTTLE, PLASTIC | | 2018-09-01 | 0000-00-00 | No | No | Current |