Package 58602-845-21

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 58602-845-21
Digits Only 5860284521
Product NDC 58602-845
Description

1 BOTTLE in 1 CARTON (58602-845-21) / 100 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-05-16
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": "58b5f12c-9192-4b1a-8fe7-a9b039f909ac", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["d570f8f3-88b8-408d-8d20-3ca5f64c81f8"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-845-21)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-845-21", "marketing_start_date": "20200516"}], "brand_name": "Naproxen Sodium", "product_id": "58602-845_58b5f12c-9192-4b1a-8fe7-a9b039f909ac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "58602-845", "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": "20200516", "listing_expiration_date": "20261231"}