methylphenidate hydrochloride
NDC 0591-3902 · Actavis Pharma, Inc.
Packages
0591-3902-19 — 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0591-3902-19)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0527-6581 — methylphenidate hydrochloride, 0527-6582 — methylphenidate hydrochloride, 0527-6583 — methylphenidate hydrochloride, 0527-6584 — methylphenidate hydrochloride, 0591-3854 — methylphenidate hydrochloride, 0591-3862 — methylphenidate hydrochloride, 0591-3869 — methylphenidate hydrochloride, 0591-3873 — methylphenidate hydrochloride, 0591-3891 — methylphenidate hydrochloride, 0591-3895 — methylphenidate hydrochloride, 0781-2361 — methylphenidate, 0781-2362 — methylphenidate, 0781-2363 — methylphenidate, 0781-2364 — methylphenidate, 0781-2383 — methylphenidate, 0781-2384 — methylphenidate, 0781-2385 — methylphenidate, 0781-2386 — methylphenidate, 10702-075 — methylphenidate hydrochloride extended release, 10702-076 — methylphenidate hydrochloride extended release, +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