Acetaminophen

NDC 0615-8250 · NCS HealthCare of KY, LLC dba Vangard Labs

Generic nameAcetaminophen

Dosage formTABLET

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength500 mg/1

Marketing categoryOTC MONOGRAPH DRUG

Packages

0615-8250-05 — 15 TABLET in 1 BLISTER PACK (0615-8250-05)

0615-8250-39 — 30 TABLET in 1 BLISTER PACK (0615-8250-39)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0536-1376 — Acetaminophen and Ibuprofen, 0536-1413 — Acetaminophen, 0536-1426 — Acetaminophen, 0573-0145 — Ibuprofen, Acetaminophen, 0573-0147 — Ibuprofen, Acetaminophen, 0591-2640 — Butalbital, Acetaminophen, and Caffeine, 0591-2641 — Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate, 0591-3220 — Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate, 0591-3369 — Butalbital, Acetaminophen, and Caffeine, 0603-2540 — butalbital and acetaminophen, 0615-8397 — ACETAMINOPHEN, 0615-8398 — ACETAMINOPHEN, 0615-8608 — ACETAMINOPHEN, 0615-8609 — ACETAMINOPHEN, 0615-8610 — ACETAMINOPHEN, 0615-8624 — ACETAMINOPHEN, 0781-3156 — acetaminophen, 0781-9274 — acetaminophen, 0904-1987 — Acetaminophen, 0904-5786 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, +3478 more

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