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NDC 41163-434 · United Natural Foods, Inc. dba UNFI

Generic nameCaffeine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)CAFFEINE
Strength200 mg/1
Pharmacologic classCentral Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
Marketing categoryOTC MONOGRAPH DRUG

Packages

41163-434-11 — 1 BOTTLE, PLASTIC in 1 CARTON (41163-434-11) / 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

36800-934 — Acetaminophen, Aspirin, Caffeine, 37808-374 — Acetaminophen, Aspirin, Caffeine, 37808-389 — Acetaminophen, Caffeine, Pyrilamine maleate, 37808-586 — Acetaminophen, Aspirin, Caffeine, 37835-531 — Acetaminophen, Aspirin, and Caffeine, 41163-226 — Caffeine, 41163-334 — acetaminophen, aspirin, caffeine, 41163-374 — Acetaminophen, Aspirin, Caffeine, 41163-390 — Acetaminophen, Caffeine and Pyrilamine maleate, 41163-391 — Acetaminophen, Caffeine, Pyrilamine maleate, 41226-370 — ACETAMINOPHEN, ASPIRIN AND CAFFEINE, 41250-143 — Aspirin, Caffeine, 41250-334 — Acetaminophen, Aspirin, Caffeine, 41250-374 — Acetaminophen, Aspirin, Caffeine, 41520-374 — Acetaminophen, Aspirin, Caffeine, 42291-181 — Butalbital, Acetaminophen, and Caffeine, 42364-0011 — acetaminophen, aspirin, and caffeine, 42364-2208 — acetaminophen, aspirin, and caffeine, 42507-374 — Acetaminophen, Aspirin, Caffeine, 42961-234 — Acetaminophen Aspirin Caffeine, +468 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.

T43.611 — Poisoning by caffeine, accidental (unintentional), T43.612 — Poisoning by caffeine, intentional self-harm, T43.613 — Poisoning by caffeine, assault, T43.614 — Poisoning by caffeine, undetermined, T43.615 — Adverse effect of caffeine, T43.616 — Underdosing of caffeine

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.