Package 69230-329-05

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 69230-329-05
Digits Only 6923032905
Product NDC 69230-329
Description

500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05)

Marketing

Marketing Status
Marketed Since 2022-10-28
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"}