Tilia Fe
NDC 51862-896, NdAc and EE Tablets and Ferrous Fumarate Tablets, kit, from Mayne Pharma Inc..
- Product NDC
- 51862-896
- Status
- Listed
- Labeler
- Mayne Pharma Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202962
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51862-896 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51862-896-01 | 51862089601 | 1 BLISTER PACK in 1 PACKET (51862-896-01) / 1 KIT in 1 BLISTER PACK |
| 51862-896-02 | 51862089602 | 1 BLISTER PACK in 1 CARTON (51862-896-02) / 1 KIT in 1 BLISTER PACK |
| 51862-896-06 | 51862089606 | 6 BLISTER PACK in 1 CARTON (51862-896-06) / 1 KIT in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/cebfb589-1b34-4f51-a0c8-c2c0cf4c7145
Use it
Look up 51862-896 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51862-896 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51862-896. 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.