United States · FDA National Drug Code directory
Methylphenidate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0781-2364_2a42277a-d670-4bae-b49d-fd1d8e13afff
- Product NDC
- 0781-2364
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- methylphenidate
- Labeler
- Sandoz Inc
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20151124 / 20270430
Source-listed ingredients
- METHYLPHENIDATE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2364-01) · 0781-2364-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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