good sense naproxen sodium

Generic: naproxen sodium

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name good sense naproxen sodium
Generic Name naproxen sodium
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8443
Product ID 68788-8443_f166dfdc-9b33-430b-bf6b-46310f9ea708
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 2023-05-10

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 687888443
Hyphenated Format 68788-8443

Supplemental Identifiers

RxCUI
849574
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 good sense 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
  • 20 TABLET, FILM COATED in 1 BOTTLE (68788-8443-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8443-3)
  • 40 TABLET, FILM COATED in 1 BOTTLE (68788-8443-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-8443-6)
source: ndc

Packages (4)

68788-8443-2 20 TABLET, FILM COATED in 1 BOTTLE (68788-8443-2) 68788-8443-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-8443-3) 68788-8443-4 40 TABLET, FILM COATED in 1 BOTTLE (68788-8443-4) 68788-8443-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-8443-6)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Good Sense Naproxen Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f166dfdc-9b33-430b-bf6b-46310f9ea708", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["2183df53-ac90-4d43-8a5d-8421036bc4cb"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8443-2)", "package_ndc": "68788-8443-2", "marketing_start_date": "20230510"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8443-3)", "package_ndc": "68788-8443-3", "marketing_start_date": "20230510"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68788-8443-4)", "package_ndc": "68788-8443-4", "marketing_start_date": "20230510"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8443-6)", "package_ndc": "68788-8443-6", "marketing_start_date": "20230510"}], "brand_name": "Good Sense Naproxen Sodium", "product_id": "68788-8443_f166dfdc-9b33-430b-bf6b-46310f9ea708", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8443", "generic_name": "Naproxen Sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Good Sense Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20230510", "listing_expiration_date": "20261231"}