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Tagamet

NDC 63029-223 · Medtech Products Inc.

Generic nameCimetidine
Dosage formTABLET
RouteORAL
Active ingredient(s)CIMETIDINE
Strength200 mg/1
Pharmacologic classHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Marketing categoryNDA

Packages

63029-223-30 — 3 BLISTER PACK in 1 BOX (63029-223-30) / 10 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55289-581 — cimetidine, 59640-022 — Cimetidine, 59651-823 — CIMETIDINE, 59651-824 — CIMETIDINE, 59651-825 — CIMETIDINE, 59651-826 — CIMETIDINE, 59779-022 — Cimetidine, 62135-630 — CIMETIDINE, 62135-631 — CIMETIDINE, 62135-632 — CIMETIDINE, 62135-633 — CIMETIDINE, 63029-222 — Cimetidine, 63187-333 — Cimetidine, 63629-1783 — Cimetidine, 69452-323 — cimetidine, 69452-324 — cimetidine, 69452-325 — cimetidine, 69452-326 — cimetidine, 72288-022 — Cimetidine, 72288-470 — 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