Allergy Relief
NDC 37808-392, Fexofenadine Hydrochloride, tablet, from HEB.
- Product NDC
- 37808-392
- Status
- Listed
- Labeler
- HEB
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA211075
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/37808-392 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FEXOFENADINE HYDROCHLORIDE180 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 37808-392-03 | 37808039203 | 3 BLISTER PACK in 1 CARTON (37808-392-03) / 5 TABLET in 1 BLISTER PACK |
| 37808-392-17 | 37808039217 | 1 BOTTLE, PLASTIC in 1 CARTON (37808-392-17) / 30 TABLET in 1 BOTTLE, PLASTIC |
| 37808-392-18 | 37808039218 | 1 BOTTLE, PLASTIC in 1 CARTON (37808-392-18) / 40 TABLET in 1 BOTTLE, PLASTIC |
| 37808-392-19 | 37808039219 | 1 BOTTLE, PLASTIC in 1 CARTON (37808-392-19) / 45 TABLET in 1 BOTTLE, PLASTIC |
| 37808-392-20 | 37808039220 | 90 TABLET in 1 BOTTLE, PLASTIC (37808-392-20) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 37808-392 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/37808-392 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 37808-392. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.