United States · FDA National Drug Code directory
Dexmethylphenidate 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
- 27808-093_9e21f04a-b4b6-45b8-8da3-5955e6aa18a5
- Product NDC
- 27808-093
- Form
- TABLET
- Composition / generic term
- dexmethylphenidate hydrochloride
- Labeler
- Cranbury Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20011130
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXMETHYLPHENIDATE HYDROCHLORIDE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (27808-093-01) · 27808-093-01
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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