Modafinil
NDC 71610-685, modafinil, tablet, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-685
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077667
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/71610-685 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MODAFINIL200 mg/1
Pharmacologic classes
Central Nervous System Stimulation [PE]; Increased Sympathetic Activity [PE]; Sympathomimetic-like Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-685-30 | 71610068530 | 30 TABLET in 1 BOTTLE (71610-685-30) |
| 71610-685-53 | 71610068553 | 60 TABLET in 1 BOTTLE (71610-685-53) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a4a27496-0f5a-4ea8-b48c-72fcb323dc8f
Use it
Look up 71610-685 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-685 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-685. 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.