Skip to main content

CIMETIDINE

NDC 62135-631 · Chartwell RX, LLC

Generic nameCIMETIDINE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CIMETIDINE
Strength300 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryANDA

Packages

62135-631-90 — 90 TABLET, FILM COATED in 1 BOTTLE (62135-631-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-697 — cimetidine, 52183-223 — cimetidine, 55289-581 — cimetidine, 59640-022 — Cimetidine, 59651-823 — CIMETIDINE, 59651-824 — CIMETIDINE, 59651-825 — CIMETIDINE, 59651-826 — CIMETIDINE, 59779-022 — Cimetidine, 62135-630 — CIMETIDINE, 62135-632 — CIMETIDINE, 62135-633 — CIMETIDINE, 63029-222 — Cimetidine, 63029-223 — Cimetidine, 63187-333 — Cimetidine, 63629-1783 — Cimetidine, 69452-323 — cimetidine, 69452-324 — cimetidine, 69452-325 — cimetidine, 69452-326 — cimetidine, +14 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.

T47.0X1 — Poisoning by histamine H2-receptor blockers, accidental (unintentional), T47.0X2 — Poisoning by histamine H2-receptor blockers, intentional self-harm, T47.0X3 — Poisoning by histamine H2-receptor blockers, assault, T47.0X4 — Poisoning by histamine H2-receptor blockers, undetermined, T47.0X5 — Adverse effect of histamine H2-receptor blockers, T47.0X6 — Underdosing of histamine H2-receptor blockers