Allergy Relief
- Product NDC
- 36800-652
- 11-digit product format
- 368000652
- Labeler code
- 36800
- Product ID
- 36800-652_d0e84032-1758-4467-e053-2a95a90a2d74
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TopCo Associates LLC
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2018-05-12
- Marketing end
- 2023-04-30
- 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 |
|---|
| 36800-652-14 | 36800065214 | 180 TABLET in 1 BOTTLE, PLASTIC (36800-652-14) | 180 tablet | 2019-01-29 | 0000-00-00 | No | No | Current |
| 36800-652-16 | 36800065216 | 2 BOTTLE, PLASTIC in 1 CARTON (36800-652-16) > 30 TABLET in 1 BOTTLE, PLASTIC | | 2019-01-29 | 0000-00-00 | No | No | Current |