up and up allergy relief
- Product NDC
- 11673-617
- 11-digit product format
- 116730617
- Labeler code
- 11673
- Product ID
- 11673-617_642da0b5-69e6-4219-ae21-a5443b5fba2c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA212971
- Marketing category
- ANDA
- Marketing start
- 2021-09-17
- 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 |
|---|
| 11673-617 | UP AND UP ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [TARGET CORPORATION] | 2 | Legacy NDC | 20211028_4f72589d-57e7-4c61-b29c-80636f0bd220.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-617-00 | 11673061700 | 1 BOTTLE in 1 CARTON (11673-617-00) > 40 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-09-30 | 0000-00-00 | No | No | Current |
| 11673-617-01 | 11673061701 | 1 BOTTLE in 1 CARTON (11673-617-01) > 70 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-09-30 | 0000-00-00 | No | No | Current |
| 11673-617-22 | 11673061722 | 15 BLISTER PACK in 1 CARTON (11673-617-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 15 blister pack | 2021-09-30 | 0000-00-00 | No | No | Current |
| 11673-617-39 | 11673061739 | 1 BOTTLE in 1 CARTON (11673-617-39) > 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-09-17 | 0000-00-00 | No | No | Current |
| 11673-617-47 | 11673061747 | 1 BOTTLE in 1 CARTON (11673-617-47) > 150 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-09-30 | 0000-00-00 | No | No | Current |