Arthritis Pain

NDC 42507-205 · HYVEE INC

Generic nameAcetaminophen

Dosage formTABLET, EXTENDED RELEASE

RouteORAL

Active ingredient(s)ACETAMINOPHEN

Strength650 mg/1

Marketing categoryANDA

Packages

42507-205-01 — 1 BOTTLE, PLASTIC in 1 CARTON (42507-205-01) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

42507-205-02 — 1 BOTTLE, PLASTIC in 1 CARTON (42507-205-02) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

42507-205-03 — 1 BOTTLE, PLASTIC in 1 CARTON (42507-205-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

42507-205-05 — 150 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42507-205-05)

42507-205-09 — 225 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42507-205-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42364-2208 — acetaminophen, aspirin, and caffeine, 42507-001 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 42507-020 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 42507-056 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 42507-095 — Acetaminophen and Diphenhydramine Hydrochloride, 42507-103 — Acetaminophen, 42507-148 — Acetaminophen, 42507-163 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-170 — Acetaminophen, 42507-173 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-219 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-223 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 42507-278 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-303 — Acetaminophen, 42507-320 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 42507-374 — Acetaminophen, Aspirin, Caffeine, 42507-375 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-401 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 42507-404 — Acetaminophen, 42507-437 — Acetaminophen, Diphenhydramine HCl, +3476 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