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Arthritis Pain

NDC 53943-200 · DISCOUNT DRUG MART

Generic nameAcetaminophen
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)ACETAMINOPHEN
Strength650 mg/1
Marketing categoryANDA

Packages

53943-200-02 — 1 BOTTLE, PLASTIC in 1 CARTON (53943-200-02) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

53943-200-03 — 1 BOTTLE, PLASTIC in 1 PACKAGE (53943-200-03) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

53943-200-09 — 225 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53943-200-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53943-104 — Acetaminophen, 53943-138 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 53943-163 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-167 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-170 — Acetaminophen, 53943-175 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-178 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-197 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-198 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-199 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-201 — Acetaminophen, 53943-220 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 53943-228 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 53943-239 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE, 53943-274 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-298 — Acetaminophen, 53943-304 — Acetaminophen, 53943-305 — ACETAMINOPHEN, ASPIRIN and CAFFEINE, 53943-319 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 53943-323 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, +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