naproxen sodium

Generic: naproxen sodium

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

naproxen sodium 375 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-252
Product ID 24979-252_a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA020353
Listing Expiration 2026-12-31
Marketing Start 2024-04-25

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 24979252
Hyphenated Format 24979-252

Supplemental Identifiers

RxCUI
1116320 1116339 1116349
UPC
0324979252018 0324979254067 0324979253688
UNII
9TN87S3A3C

Packaging Origin

Original Packager
true

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 naproxen sodium (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number NDA020353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 375 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-252-01)
source: ndc

Packages (1)

24979-252-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-252-01)

Ingredients (1)

naproxen sodium (375 mg/1)

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927", "openfda": {"upc": ["0324979252018", "0324979254067", "0324979253688"], "unii": ["9TN87S3A3C"], "rxcui": ["1116320", "1116339", "1116349"], "spl_set_id": ["7c22a2d6-821c-4f83-aead-e756aed930e5"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-252-01)", "package_ndc": "24979-252-01", "marketing_start_date": "20240425"}], "brand_name": "Naproxen Sodium", "product_id": "24979-252_a79a3bf0-fe2f-4ba4-8eaa-e1c97ab9b927", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "24979-252", "generic_name": "Naproxen Sodium", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "375 mg/1"}], "application_number": "NDA020353", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240425", "listing_expiration_date": "20261231"}