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Naprelan

NDC 24979-249 · Upsher-Smith Laboratories, LLC

Generic nameNaproxen Sodium
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)NAPROXEN SODIUM
Strength375 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryNDA

Packages

24979-249-01 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-249-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-180 — Naproxen Sodium, 21130-593 — Naproxen Sodium, 21130-608 — Naproxen sodium, 21130-639 — diphenhydramine hydrochloride, naproxen sodium, 21130-674 — Naproxen Sodium, 21130-690 — Naproxen Sodium, 21130-748 — Naproxen Sodium, 21130-814 — Naproxen Sodium Diphenhydramine Hydrochloride, 21130-856 — Naproxen Sodium, 21130-948 — 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, 27854-170 — Naproxen Sodium, +318 more

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