Package 69230-329-50
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
69230-329-50
Digits Only
6923032950
Product NDC
69230-329
Description
1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
naproxen sodium
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee21e0f7-9f32-6c63-e053-2a95a90ac996", "openfda": {"upc": ["0369230329016"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["d1008e19-ff0d-4ed2-909d-bae5a82a1234"], "manufacturer_name": ["Camber Consumer Care Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69230-329-01", "marketing_start_date": "20221028"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69230-329-02", "marketing_start_date": "20221028"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05)", "package_ndc": "69230-329-05", "marketing_start_date": "20221028"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10)", "package_ndc": "69230-329-10", "marketing_start_date": "20221028"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69230-329-24", "marketing_start_date": "20221028"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69230-329-50", "marketing_start_date": "20221028"}], "brand_name": "Naproxen sodium", "product_id": "69230-329_ee21e0f7-9f32-6c63-e053-2a95a90ac996", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69230-329", "generic_name": "Naproxen sodium", "labeler_name": "Camber Consumer Care Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA211065", "marketing_category": "ANDA", "marketing_start_date": "20221028", "listing_expiration_date": "20261231"}