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
72162-2086_11f4ec97-ed86-48b5-af3a-446b882294cb
Product NDC
72162-2086
Form
TABLET
Composition / generic term
METHYLPHENIDATE HYDROCHLORIDE
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20140407
Source listing expiry
20261231

Source-listed ingredients

  • METHYLPHENIDATE HYDROCHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (72162-2086-1) · 72162-2086-1

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →