naproxen sodium

Generic: naproxen sodium

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-596
Product ID 63187-596_056f2617-2de4-4296-bd4d-714f34f7a15c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 2014-04-11

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 63187596
Hyphenated Format 63187-596

Supplemental Identifiers

RxCUI
849574
UPC
0363187596309
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 naproxen sodium (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA074661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 24 TABLET, FILM COATED in 1 BOTTLE (63187-596-24)
  • 28 TABLET, FILM COATED in 1 BOTTLE (63187-596-28)
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-596-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-596-60)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-596-90)
source: ndc

Packages (5)

63187-596-24 24 TABLET, FILM COATED in 1 BOTTLE (63187-596-24) 63187-596-28 28 TABLET, FILM COATED in 1 BOTTLE (63187-596-28) 63187-596-30 30 TABLET, FILM COATED in 1 BOTTLE (63187-596-30) 63187-596-60 90 TABLET, FILM COATED in 1 BOTTLE (63187-596-60) 63187-596-90 60 TABLET, FILM COATED in 1 BOTTLE (63187-596-90)

Ingredients (1)

naproxen sodium (220 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": "056f2617-2de4-4296-bd4d-714f34f7a15c", "openfda": {"upc": ["0363187596309"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["e668c80f-dd53-4b82-8678-5e4fccb13023"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (63187-596-24)", "package_ndc": "63187-596-24", "marketing_start_date": "20170901"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (63187-596-28)", "package_ndc": "63187-596-28", "marketing_start_date": "20170801"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-596-30)", "package_ndc": "63187-596-30", "marketing_start_date": "20150803"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-596-60)", "package_ndc": "63187-596-60", "marketing_start_date": "20150803"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-596-90)", "package_ndc": "63187-596-90", "marketing_start_date": "20150803"}], "brand_name": "Naproxen Sodium", "product_id": "63187-596_056f2617-2de4-4296-bd4d-714f34f7a15c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63187-596", "generic_name": "Naproxen Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20140411", "listing_expiration_date": "20261231"}