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Mucinex

NDC 72854-223 · Reckitt Benckiser LLC

Generic nameNaproxen Sodium, Pseudoephedrine Hydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)NAPROXEN SODIUM, PSEUDOEPHEDRINE HYDROCHLORIDE
Strength220; 120 mg/1; mg/1
Pharmacologic classAdrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC]
Marketing categoryANDA

Packages

72854-223-20 — 2 BLISTER PACK in 1 CARTON (72854-223-20) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72288-310 — diphenhydramine hydrochloride, naproxen sodium, 72288-312 — Naproxen Sodium, 72288-331 — Naproxen Sodium, 72288-366 — Naproxen Sodium, 72288-368 — Naproxen Sodium, 72288-489 — Naproxen Sodium, 72476-748 — Naproxen Sodium, 72789-389 — Naproxen Sodium, 72789-543 — Naproxen Sodium, 72854-001 — Naproxen Sodium, Dextromethorphan Hydrobromide, Guaifenesin, 75907-207 — Brompheniramine Maleate, Pseudoephedrine Hydrochloride, and Dextromethorphan Hydrobromide, 76162-801 — guaifenesin and pseudoephedrine hydrochloride, 76420-627 — Naproxen Sodium, 76420-637 — Naproxen Sodium, 79481-0119 — guaifenesin and pseudoephedrine hydrochloride, 79481-0709 — guaifenesin and pseudoephedrine hydrochloride, 79481-1002 — Guaifenesin and Pseudoephedrine HCl, 79903-005 — Naproxen Sodium, 79903-108 — Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, 79903-125 — guaifenesin and pseudoephedrine hydrochloride, +606 more

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 Q3 (July 2026 release). All data sources · How to read the labels