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DOLONEURO-TROPAS

NDC 69729-795 · OPMX LLC

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameAcetaminophen, Caffeine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, CAFFEINE
Strength500; 65 mg/1; mg/1
Pharmacologic classCentral Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69729-795-24 — 2 BLISTER PACK in 1 CARTON (69729-795-24) / 12 TABLET, FILM COATED in 1 BLISTER PACK

69729-795-80 — 20 BLISTER PACK in 1 CARTON (69729-795-80) / 4 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69729-323 — Acetaminophen, Chlorpheniramine Maleate, Phenylephrine HCl, 69729-601 — Acetaminophen, Aspirin, Caffeine, 69729-782 — Acetaminophen, Guaifenesin, Dextromethorphan HBr, Phenylephrine HCl, 69729-784 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69729-785 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69729-786 — Acetaminophen, Dextromethorphan HBr, Guafeisin USP, Phenylephrine HCl, 69729-787 — Acetaminophen, Dextromethorphan HBr, Guaifenesin USP, Phenylephrine HCl, 69729-789 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin USP, Phenylephrine Hydrochloride, 69729-790 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin USP, Phenylephrine Hydrochloride, 69729-793 — Acetaminophen, Caffeine, 69729-800 — Acetaminophen, 69729-801 — Acetaminophen, 69729-802 — Acetaminophen, Dextomethorphan Hydrobromide, Phenylephrine Hydrochloride, 69729-808 — Acetaminohpen, Dextromethorphan Hydrobromide, 69729-809 — Acetaminophen, Dextromethorphan Hydrobromide, 69729-813 — Acetaminophen, Caffeine and Pyrilamine Maleate, 69729-815 — Acetaminophen, 69729-816 — Acetaminophen, Dextromethorphan Hydrobromide, 69729-818 — Acetaminophen, Caffeine, Pyrilamine maleate, 69729-825 — Acetaminophen, +3610 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q4 (October 2026 release). All data sources · How to read the labels

Current data releases:ICD-10-CM FY2027 · ICD-10-PCS FY2027 · HCPCS October 2026 · MS-DRG v44 · Medicare Code Editor v44.0 · NCCI PTP Q4 2026 · MUE Q4 2026 · NCD code lists 2026-01 · LCD export September 28, 2026 · All releases and sources