fludrocortisone acetate
NDC 71930-088, fludrocortisone acetate, tablet, from Eywa Pharma Inc.
- Product NDC
- 71930-088
- Status
- Listed
- Labeler
- Eywa Pharma Inc
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA220308
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71930-088 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUDROCORTISONE ACETATE.1 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71930-088-12 | 71930008812 | 100 TABLET in 1 BOTTLE (71930-088-12) |
| 71930-088-52 | 71930008852 | 500 TABLET in 1 BOTTLE (71930-088-52) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/eff2eae8-94ce-46ca-a027-6b1d08e7b96bNADAC price for package 71930008812
GET /v1/drugs/nadac/71930008812NADAC price for package 71930008852
GET /v1/drugs/nadac/71930008852
Use it
Look up 71930-088 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71930-088 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71930-088. 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.