up and up allergy relief
- Product NDC
- 11673-800
- 11-digit product format
- 116730800
- Labeler code
- 11673
- Product ID
- 11673-800_9c79e2b5-1381-48bd-a324-372d856745c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA076447
- Marketing category
- ANDA
- Marketing start
- 2015-03-25
- 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 |
|---|
| 11673-800-33 | 11673080033 | 1 BOTTLE in 1 CARTON (11673-800-33) > 60 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-03-25 | 0000-00-00 | No | No | Current |
| 11673-800-46 | 11673080046 | 10 BLISTER PACK in 1 CARTON (11673-800-46) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2015-03-25 | 0000-00-00 | No | No | Current |