Skip to main content

Methylphenidate Hydrochloride

NDC 72603-399 · Northstar Rx LLC

Generic nameMethylphenidate Hydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)METHYLPHENIDATE HYDROCHLORIDE
Strength72 mg/1
Pharmacologic classCentral Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
DEA scheduleCII
Marketing categoryANDA

Packages

72603-399-01 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72603-399-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 72162-2430 — METHYLPHENIDATE HYDROCHLORIDE, 72865-122 — METHYLPHENIDATE HYDROCHLORIDE, 72865-123 — METHYLPHENIDATE HYDROCHLORIDE, 72865-124 — METHYLPHENIDATE HYDROCHLORIDE, 72865-125 — Methylphenidate Hydrochloride, 72865-126 — Methylphenidate Hydrochloride, 72865-127 — Methylphenidate Hydrochloride, 72865-133 — Methylphenidate Hydrochloride, 72865-134 — Methylphenidate Hydrochloride, 72865-135 — Methylphenidate Hydrochloride, 72865-136 — 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 August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.