allergy relief
- Product NDC
- 11822-0425
- 11-digit product format
- 118220425
- Labeler code
- 11822
- Product ID
- 11822-0425_81352698-6cc8-49b6-ab9f-ddd62ff8d75e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA076447
- Marketing category
- ANDA
- Marketing start
- 2020-08-01
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 60 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0425 | ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [RITE AID CORPORATION] | 3 | Legacy NDC | 20210605_93bdf7ff-4139-450e-a7bd-6c5a957b14ca.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0425-0 | 11822042500 | 24 BLISTER PACK in 1 CARTON (11822-0425-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 24 blister pack | 2020-08-01 | 0000-00-00 | No | No | Current |