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AnaDent

NDC 27854-170 · Belmora LLC

Generic nameNaproxen Sodium
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)NAPROXEN SODIUM
Strength220 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

27854-170-01 — 1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

24979-249 — Naproxen Sodium, 24979-250 — Naproxen Sodium, 24979-251 — Naproxen Sodium, 24979-252 — Naproxen Sodium, 24979-253 — Naproxen Sodium, 24979-254 — Naproxen Sodium, 25000-141 — Naproxen Sodium, Coated Tablets, 25000-144 — Naproxen Sodium Tablet, coated, 27854-160 — Naproxen Sodium, 27854-165 — Naproxen Sodium, 27854-505 — Naproxen Sodium, 27854-555 — Naproxen Sodium, 27854-700 — Naproxen sodium, 27854-701 — Naproxen Sodium, 30142-285 — Naproxen Sodium, 30142-753 — diphenhydramine hydrochloride, naproxen sodium, 30142-954 — Naproxen Sodium, 36800-140 — Naproxen sodium, 36800-204 — Naproxen Sodium, 36800-264 — diphenhydramine hydrochloride, naproxen sodium, +318 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