Allegra Allergy, Travel BASIX
- Product NDC
- 66715-6507
- 11-digit product format
- 667156507
- Labeler code
- 66715
- Product ID
- 66715-6507_5076f5eb-2ebc-5623-e063-6394a90a3fff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lil' Drug Store Products, Inc
- Application
- NDA020872
- Marketing category
- NDA
- Marketing start
- 2022-10-11
- 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
- 2027-12-31
- 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 |
|---|
| 66715-6507-2 | 66715650702 | 2 BLISTER PACK in 1 CARTON (66715-6507-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2022-10-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allegra ® Allergy | Lil' Drug Store Products, Inc | 2026-04-27 | HUMAN OTC DRUG LABEL | 9 |