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All Day Pain Relief

NDC 37808-068 · H E B

Generic nameNaproxen Sodium
Dosage formTABLET
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

37808-068-24 — 1 BOTTLE, PLASTIC in 1 BOX (37808-068-24) / 24 TABLET in 1 BOTTLE, PLASTIC

37808-068-50 — 1 BOTTLE, PLASTIC in 1 BOX (37808-068-50) / 50 TABLET in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

30142-753 — diphenhydramine hydrochloride, naproxen sodium, 30142-954 — Naproxen Sodium, 36800-140 — Naproxen sodium, 36800-204 — Naproxen Sodium, 36800-264 — diphenhydramine hydrochloride, naproxen sodium, 36800-368 — Naproxen Sodium, 36800-417 — Naproxen sodium, Pseudoephedrine HCl, 36800-490 — Naproxen Sodium, 36800-696 — naproxen sodium, 37808-049 — Naproxen Sodium, 37808-264 — diphenhydramine hydrochloride, naproxen sodium, 37808-631 — Naproxen sodium, 37808-652 — Naproxen Sodium, 37808-713 — Naproxen Sodium, 37835-594 — Naproxen Sodium, 41163-079 — Naproxen Sodium, 41163-511 — Naproxen Sodium, 41163-593 — diphenhydramine hydrochloride, naproxen sodium, 41163-707 — Naproxen Sodium, 41226-609 — 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.

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