allergy relief
- Product NDC
- 0363-7011
- 11-digit product format
- 003637011
- Labeler code
- 0363
- Product ID
- 0363-7011_0d3aa246-3316-4686-b69c-330ef3b21fcd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA212971
- Marketing category
- ANDA
- Marketing start
- 2024-02-08
- 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 |
|---|
| 0363-7011-39 | 00363701139 | 1 BOTTLE in 1 CARTON (0363-7011-39) / 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2024-02-08 | No | No | Historical |