Methylphenidate Hydrochloride
NDC 72603-399, Methylphenidate Hydrochloride, tablet, extended release, from Northstar Rx LLC.
- Product NDC
- 72603-399
- Status
- Listed
- Labeler
- Northstar Rx LLC
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217229
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72603-399 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYLPHENIDATE HYDROCHLORIDE72 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72603-399-01 | 72603039901 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72603-399-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/768bf181-d0d8-49e5-9c87-cacbb069e0b2NADAC price for package 72603039901
GET /v1/drugs/nadac/72603039901
Use it
Look up 72603-399 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72603-399 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72603-399. 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.