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
- 43386-573_ac26e6b6-2be0-458d-8acc-d963bcca13a5
- Product NDC
- 43386-573
- Form
- TABLET
- Composition / generic term
- Methylphenidate Hydrochloride
- Labeler
- Lupin Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160120
- Source listing expiry
- 20261231
Source-listed ingredients
- METHYLPHENIDATE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (43386-573-01) · 43386-573-01
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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