aleve caplets

Generic: naproxen sodium

Labeler: select consumer group
NDC Directory HUMAN OTC DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name aleve caplets
Generic Name naproxen sodium
Labeler select consumer group
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Select Consumer Group

Identifiers & Regulatory

Product NDC 85237-1832
Product ID 85237-1832_46fdc753-1f23-d8ce-e063-6294a90a86e5
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA020204
Listing Expiration 2026-12-31
Marketing Start 2023-04-04

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 852371832
Hyphenated Format 85237-1832

Supplemental Identifiers

RxCUI
849574 849728
UPC
0025866592049 0025866592339
UNII
9TN87S3A3C

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name aleve caplets (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number NDA020204 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 POUCH in 1 BLISTER PACK (85237-1832-1) / 1 TABLET in 1 POUCH
  • 2 POUCH in 1 BLISTER PACK (85237-1832-2) / 1 TABLET in 1 POUCH
  • 25 POUCH in 1 BOX, UNIT-DOSE (85237-1832-4) / 1 TABLET in 1 POUCH
  • 50 POUCH in 1 BOX, UNIT-DOSE (85237-1832-6) / 1 TABLET in 1 POUCH
source: ndc

Packages (4)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46fdc753-1f23-d8ce-e063-6294a90a86e5", "openfda": {"upc": ["0025866592049", "0025866592339"], "unii": ["9TN87S3A3C"], "rxcui": ["849574", "849728"], "spl_set_id": ["3ca84972-f8c9-1881-e063-6294a90a9070"], "manufacturer_name": ["Select Consumer Group"]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 BLISTER PACK (85237-1832-1)  / 1 TABLET in 1 POUCH", "package_ndc": "85237-1832-1", "marketing_start_date": "20240325"}, {"sample": false, "description": "2 POUCH in 1 BLISTER PACK (85237-1832-2)  / 1 TABLET in 1 POUCH", "package_ndc": "85237-1832-2", "marketing_start_date": "20251224"}, {"sample": false, "description": "25 POUCH in 1 BOX, UNIT-DOSE (85237-1832-4)  / 1 TABLET in 1 POUCH", "package_ndc": "85237-1832-4", "marketing_start_date": "20251224"}, {"sample": false, "description": "50 POUCH in 1 BOX, UNIT-DOSE (85237-1832-6)  / 1 TABLET in 1 POUCH", "package_ndc": "85237-1832-6", "marketing_start_date": "20251224"}], "brand_name": "Aleve Caplets", "product_id": "85237-1832_46fdc753-1f23-d8ce-e063-6294a90a86e5", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "85237-1832", "generic_name": "NAPROXEN SODIUM", "labeler_name": "Select Consumer Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aleve", "brand_name_suffix": "Caplets", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "NDA020204", "marketing_category": "NDA", "marketing_start_date": "20230404", "listing_expiration_date": "20261231"}