Fexofenadine hydrochloride
NDC 55111-782, Fexofenadine hydrochloride, tablet, from Dr. Reddy's Laboratories Limited.
- Product NDC
- 55111-782
- Status
- Listed
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA076502
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/55111-782 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FEXOFENADINE HYDROCHLORIDE30 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 55111-782-01 | 55111078201 | 100 TABLET in 1 BOTTLE (55111-782-01) |
| 55111-782-30 | 55111078230 | 30 TABLET in 1 BOTTLE (55111-782-30) |
| 55111-782-78 | 55111078278 | 10 BLISTER PACK in 1 CARTON (55111-782-78) / 10 TABLET in 1 BLISTER PACK (55111-782-79) |
| 55111-782-90 | 55111078290 | 90 TABLET in 1 BOTTLE (55111-782-90) |
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 55111-782 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/55111-782 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 55111-782. 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.