Allergy Relief
- Product NDC
- 37012-571
- 11-digit product format
- 370120571
- Labeler code
- 37012
- Product ID
- 37012-571_7b1eb700-5881-4e56-9d51-b62b1e4784d0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hcl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC
- Application
- ANDA076447
- Marketing category
- ANDA
- Marketing start
- 2013-07-08
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 37012-571-22 | 37012057122 | 15 BLISTER PACK in 1 CARTON (37012-571-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 15 blister pack | 2013-07-08 | 0000-00-00 | No | No | Current |
| 37012-571-39 | 37012057139 | 1 BOTTLE in 1 CARTON (37012-571-39) > 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2013-10-02 | 0000-00-00 | No | No | Current |
| 37012-571-75 | 37012057175 | 1 BOTTLE in 1 CARTON (37012-571-75) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2013-07-17 | 0000-00-00 | No | No | Current |
| 37012-571-95 | 37012057195 | 1 BOTTLE in 1 CARTON (37012-571-95) > 45 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-11-30 | 0000-00-00 | No | No | Current |