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Methylphenidate Hydrochloride

NDC 72162-1992 · Bryant Ranch Prepack

Generic nameMethylphenidate Hydrochloride
Dosage formSOLUTION
RouteORAL
Active ingredient(s)METHYLPHENIDATE HYDROCHLORIDE
Strength5 mg/5mL
Pharmacologic classCentral Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
DEA scheduleCII
Marketing categoryANDA

Packages

72162-1992-5 — 500 mL in 1 BOTTLE (72162-1992-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2968 — METHYLPHENIDATE HYDROCHLORIDE, 71376-201 — Methylphenidate Hydrochloride, 71376-202 — Methylphenidate Hydrochloride, 71376-203 — Methylphenidate Hydrochloride, 71376-204 — Methylphenidate Hydrochloride, 71376-205 — Methylphenidate Hydrochloride, 71930-024 — Methylphenidate Hydrochloride, 71930-025 — Methylphenidate Hydrochloride, 72162-1306 — Methylphenidate Hydrochloride, 72162-1636 — Methylphenidate Hydrochloride, 72162-1993 — Methylphenidate Hydrochloride, 72162-2019 — METHYLPHENIDATE HYDROCHLORIDE, 72162-2040 — Methylphenidate Hydrochloride, 72162-2041 — Methylphenidate Hydrochloride, 72162-2086 — METHYLPHENIDATE HYDROCHLORIDE, 72162-2087 — METHYLPHENIDATE HYDROCHLORIDE, 72162-2394 — Methylphenidate Hydrochloride, 72162-2395 — Methylphenidate Hydrochloride, 72162-2428 — METHYLPHENIDATE HYDROCHLORIDE, 72162-2429 — METHYLPHENIDATE HYDROCHLORIDE, +213 more

Poisoning, adverse-effect and underdosing codes for this drug

The ICD-10-CM Table of Drugs and Chemicals carries these diagnosis codes for this drug — a drug-name match derived from FDA's product name and the Table of Drugs and Chemicals, not a CMS-published pairing.

T43.631 — Poisoning by methylphenidate, accidental (unintentional), T43.632 — Poisoning by methylphenidate, intentional self-harm, T43.633 — Poisoning by methylphenidate, assault, T43.634 — Poisoning by methylphenidate, undetermined, T43.635 — Adverse effect of methylphenidate, T43.636 — Underdosing of methylphenidate

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.