Methylphenidate Hydrochloride
NDC 71930-024, Methylphenidate Hydrochloride, solution, from Eywa Pharma Inc.
- Product NDC
- 71930-024
- Status
- Listed
- Labeler
- Eywa Pharma Inc
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210139
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/71930-024 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE5 mg/5mL
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71930-024-52 | 71930002452 | 500 mL in 1 BOTTLE (71930-024-52) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/298fb86d-7d94-49e1-b743-3e7801122422NADAC price for package 71930002452
GET /v1/drugs/nadac/71930002452
Use it
Look up 71930-024 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71930-024 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71930-024. 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.