Citalopram
NDC 70518-2617 · REMEDYREPACK INC.
Packages
70518-2617-0 — 30 TABLET in 1 BLISTER PACK (70518-2617-0)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
68788-0802 — Citalopram Hydrobromide, 68788-8962 — Citalopram Hydrobromide, 68788-9692 — Citalopram Hydrobromide, 68999-540 — Citalopram, 69097-822 — Citalopram, 69097-823 — Citalopram, 69097-824 — Citalopram, 70518-2228 — Citalopram, 70518-2553 — citalopram, 70518-2601 — citalopram, 70518-4114 — Citalopram Hydrobromide, 70518-4334 — Citalopram Hydrobromide, 70518-4335 — Citalopram, 70518-4416 — Citalopram, 70518-4476 — Citalopram, 71205-764 — Citalopram Hydrobromide, 71335-0238 — Citalopram Hydrobromide, 71335-0377 — Citalopram, 71335-0480 — Citalopram Hydrobromide, 71335-2232 — citalopram, +99 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.
T43.221 — Poisoning by selective serotonin reuptake inhibitors, accidental (unintentional), T43.222 — Poisoning by selective serotonin reuptake inhibitors, intentional self-harm, T43.223 — Poisoning by selective serotonin reuptake inhibitors, assault, T43.224 — Poisoning by selective serotonin reuptake inhibitors, undetermined, T43.225 — Adverse effect of selective serotonin reuptake inhibitors, T43.226 — Underdosing of selective serotonin reuptake inhibitors