United States · FDA National Drug Code directory
Methylphenidate Hydrochloride
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
- 0115-1737_b0804310-a328-4743-b417-67c66f56fc94
- Product NDC
- 0115-1737
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Methylphenidate Hydrochloride
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160920
- Source listing expiry
- 20271231
Source-listed ingredients
- METHYLPHENIDATE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0115-1737-01) · 0115-1737-01
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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