ACETAMINOPHEN

NDC 0615-8624 · NCS HealthCare of KY, LLC dba Vangard Labs

Generic nameACETAMINOPHEN

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength650 mg/1

Marketing categoryANDA

Packages

0615-8624-39 — 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8624-39)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 0615-8250 — Acetaminophen, 0615-8397 — ACETAMINOPHEN, 0615-8398 — ACETAMINOPHEN, 0615-8608 — ACETAMINOPHEN, 0615-8609 — ACETAMINOPHEN, 0615-8610 — ACETAMINOPHEN, 0781-3156 — acetaminophen, 0781-9274 — acetaminophen, 0904-1987 — Acetaminophen, 0904-5786 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 0904-5791 — Acetaminophen, 0904-5847 — Acetaminophen, 0904-6465 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0904-6645 — Acetaminophen, 0904-6720 — Acetaminophen, 0904-6730 — Acetaminophen, +3478 more

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