Skip to main content

Methylphenidate Hydrochloride (LA)

NDC 75907-053 · Dr. Reddy's Laboratories Inc

Generic nameMethylphenidate Hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)METHYLPHENIDATE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classCentral Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
DEA scheduleCII
Marketing categoryANDA

Packages

75907-053-30 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (75907-053-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-2429 — METHYLPHENIDATE HYDROCHLORIDE, 72162-2430 — METHYLPHENIDATE HYDROCHLORIDE, 72603-399 — 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, 75834-324 — METHYLPHENIDATE HYDROCHLORIDE, 75834-325 — METHYLPHENIDATE HYDROCHLORIDE, 75834-326 — METHYLPHENIDATE HYDROCHLORIDE, 75907-049 — Methylphenidate Hydrochloride, 75907-050 — Methylphenidate Hydrochloride, 75907-051 — Methylphenidate Hydrochloride, 75907-052 — 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.