Cotempla XR-ODT
NDC 70165-100 · Neos Therapeutics Brands, LLC
Packages
70165-100-30 — 5 BLISTER PACK in 1 CARTON (70165-100-30) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0378-8260 — Methylphenidate, 0378-8261 — Methylphenidate, 0378-8262 — Methylphenidate, 0378-8263 — Methylphenidate, 0574-2410 — methylphenidate, 0574-2415 — methylphenidate, 0574-2420 — methylphenidate, 0574-2430 — methylphenidate, 43602-177 — Methylphenidate Hydrochloride, 43602-178 — Methylphenidate Hydrochloride, 62542-100 — methylphenidate extended-release, 62542-250 — methylphenidate extended-release, 62542-350 — methylphenidate extended-release, 68968-5552 — methylphenidate, 68968-5553 — methylphenidate, 68968-5554 — methylphenidate, 68968-5555 — methylphenidate, 70165-200 — Methylphenidate, 70165-300 — Methylphenidate
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