fexofenadine hcl
NDC 77771-201, fexofenadine hcl, tablet, film coated, from Radha Pharmaceuticals.
- Product NDC
- 77771-201
- Status
- Listed
- Labeler
- Radha Pharmaceuticals
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA204507
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/77771-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FEXOFENADINE HYDROCHLORIDE60 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 77771-201-01 | 77771020101 | 100 TABLET, FILM COATED in 1 BOTTLE (77771-201-01) |
| 77771-201-05 | 77771020105 | 500 TABLET, FILM COATED in 1 BOTTLE (77771-201-05) |
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 77771-201 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/77771-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 77771-201. 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.