Package 58602-819-29
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
58602-819-29
Digits Only
5860281929
Product NDC
58602-819
Description
1 BOTTLE in 1 CARTON (58602-819-29) / 150 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": "915208d0-ee3a-4b1f-9c3c-76d9cb8362c9", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["46a15412-25d6-454d-86db-70321d19a2c9"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-07) / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-07", "marketing_start_date": "20211025"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-14) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-14", "marketing_start_date": "20171211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-19) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-19", "marketing_start_date": "20230921"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-21) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-21", "marketing_start_date": "20171211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-29) / 150 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-29", "marketing_start_date": "20211025"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-38) / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-38", "marketing_start_date": "20211025"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-819-40) / 500 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-819-40", "marketing_start_date": "20211025"}], "brand_name": "Naproxen Sodium", "product_id": "58602-819_915208d0-ee3a-4b1f-9c3c-76d9cb8362c9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "58602-819", "generic_name": "Naproxen Sodium", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA205497", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}