Allergy Relief
- Product NDC
- 68016-176
- 11-digit product format
- 680160176
- Labeler code
- 68016
- Product ID
- 68016-176_ef4289cb-1716-0a9c-e053-2995a90aef7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CHAIN DRUG CONSORTIUM
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2020-06-26
- Marketing end
- 2023-02-28
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68016-176-15 | 68016017615 | 1 BLISTER PACK in 1 CARTON (68016-176-15) > 15 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-06-26 | 0000-00-00 | No | No | Current |
| 68016-176-30 | 68016017630 | 1 BOTTLE, PLASTIC in 1 CARTON (68016-176-30) > 30 TABLET in 1 BOTTLE, PLASTIC | | 2020-06-26 | 0000-00-00 | No | No | Current |
| 68016-176-45 | 68016017645 | 1 BOTTLE, PLASTIC in 1 CARTON (68016-176-45) > 45 TABLET in 1 BOTTLE, PLASTIC | | 2020-06-26 | 0000-00-00 | No | No | Current |