Allergy Relief
- Product NDC
- 41250-564
- 11-digit product format
- 412500564
- Labeler code
- 41250
- Product ID
- 41250-564_f5c63072-c075-4210-9a88-2952dd6d78e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-564 | ALLERGY RELIEF (FEXOFENADINE HCL) TABLET, COATED [MEIJER, INC.] | 5 | Legacy NDC | 20230118_b9fd0873-a071-410a-85a9-5136a78dbaae.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-564-15 | 41250056415 | 15 BLISTER PACK in 1 CARTON (41250-564-15) > 1 TABLET, COATED in 1 BLISTER PACK | 15 blister pack | 2019-10-01 | 0000-00-00 | No | No | Current |
| 41250-564-90 | 41250056490 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (41250-564-90) | | 2019-10-01 | 0000-00-00 | No | No | Current |