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
- 43598-440_528a86ce-1037-944a-e934-15846984dd73
- Product NDC
- 43598-440
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Methylphenidate Hydrochloride
- Labeler
- Dr.Reddys Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200820 / 20260930
Source-listed ingredients
- METHYLPHENIDATE HYDROCHLORIDE — 36 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-440-01) · 43598-440-01
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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