Skip to main content

Caffeine

NDC 0363-5009 · Walgreen Company

Generic nameCaffeine
Dosage formTABLET
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

0363-5009-01 — 1 BOTTLE in 1 CARTON (0363-5009-01) / 100 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-0586 — Acetaminophen, Aspirin, Caffeine, 0363-0770 — ACETAMINOPHEN, ASPIRIN, CAFFEINE, 0363-0865 — Acetaminophen, Aspirin, Caffeine, 0363-1150 — Acetaminophen, Aspirin, Caffeine, 0363-1235 — acetaminophen, aspirin, caffeine, 0363-1320 — Acetaminophen 250mg Aspirin 250mg Caffeine 65mg, 0363-2310 — Acetaminophen 500mg Caffeine 60mg Pyrilamine maleate 15mg, 0363-3440 — Caffeine, 0363-3900 — Acetaminophen, Caffeine, Pyrilamine maleate, 0363-3909 — Acetaminophen, Caffeine, Pyrilamine maleate, 0363-6693 — Acetaminophen 250mg, Aspirin 250mg and Caffeine 65mg, 0363-7012 — Acetaminophen, Aspirin, Caffeine, 0363-7213 — ACETAMINOPHEN AND CAFFEINE, 0363-7214 — ACETAMINOPHEN, ASPIRIN, CAFFEINE, 0363-8712 — Aspirin and Caffeine, 0363-8992 — ACETAMINOPHEN, ASPIRIN, CAFFEINE, 0363-9390 — Acetaminophen, Caffeine, Pyrilamine maleate, 0363-9680 — Acetaminophen Aspirin Caffeine, 0517-2502 — Caffeine and Sodium Benzoate, 0527-1552 — Butalbital, aspirin, and 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.