up and up non drowsy allergy relief
- Product NDC
- 82442-300
- 11-digit product format
- 824420300
- Labeler code
- 82442
- Product ID
- 82442-300_bd226cd0-be8c-4db9-878f-5c84f6016dcc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- fexofenadine hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA212971
- Marketing category
- ANDA
- Marketing start
- 2024-03-04
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2S068B75ZU | FEXOFENADINE HYDROCHLORIDE | 153439-40-8 | FEXOFENADINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-300-72 | 82442030072 | 1 BOTTLE in 1 CARTON (82442-300-72) / 60 TABLET, COATED in 1 BOTTLE | 1 bottle | 2024-03-04 | No | No | Historical |