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NDC 68998-076 · Marc Glassman, Inc.

Generic nameCaffeine

Dosage formTABLET, 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

68998-076-84 — 2 BLISTER PACK in 1 CARTON (68998-076-84) / 8 TABLET, COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67751-145 — ACETAMINOPHEN, CAFFEINE, and PYRILAMINE MALEATE, 67751-215 — Acetaminophen, Aspirin, Caffeine, 67751-226 — caffeine, 67751-243 — Acetaminophen, Aspirin, and Caffeine, 68071-3249 — Butalbital, Acetaminophen, and Caffeine, 68071-3914 — Acetaminophen, Aspirin, Caffeine, 68163-506 — Acetaminophen, Caffeine, 68788-4126 — Butalbital, Acetaminophen and Caffeine, 68788-8137 — Butalbital, Acetaminophen, and Caffeine, 68788-8794 — BUTALBITAL, ACETAMINOPHEN AND CAFFEINE, 69168-001 — Tension Headache Relief, 69168-029 — Tension Headache Relief, 69168-076 — Caffeine, 69168-285 — Acetaminophen, Aspirin and Caffeine, 69168-470 — Menstrual Complete, 69197-029 — Acetaminophen 500 mg with Caffeine 65mg, 69238-1993 — BUTALBITAL, ASPIRIN, CAFFEINE and CODEINE PHOSPHATE, 69292-305 — butalbital, acetaminophen and caffeine, 69367-203 — Butalbital, Acetaminophen, and Caffeine, 69367-416 — 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.