Alert

NDC 49483-343 · Time Cap Labs, Inc

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 FINAL

Packages

49483-343-44 — 40 TABLET, FILM COATED in 1 BOTTLE (49483-343-44)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46122-457 — Caffeine, 46122-690 — Acetaminophen, Aspirin, Caffeine, 46672-053 — butalbital, acetaminophen and caffeine, 47682-048 — Aspirin. Caffeine, 47682-238 — Acetaminophen, Aspirin, Caffeine, 47682-821 — Aspirin,Caffeine, 47682-921 — Aspirin,Caffeine, 49035-226 — Caffeine, 49035-433 — Acetaminophen, Aspirin and Caffeine, 49035-786 — Acetaminophen, Aspirin, Caffeine, 49483-347 — Acetaminophen, Caffeine, and Pyrilamine Maleate, 49483-370 — ACETAMINOPHEN, ASPIRIN AND CAFFEINE, 49483-373 — Acetaminophen, Caffeine, 50066-630 — acetaminophen, aspirin, and caffeine, 50090-6093 — Acetaminophen, Aspirin, and Caffeine, 50090-7042 — Butalbital, Acetaminophen, and Caffeine, 50090-7519 — Butalbital, Acetaminophen and Caffeine, 50268-553 — Butalbital, Acetaminophen, and Caffeine, 50269-007 — ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE, 50269-009 — ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE, +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.