Package 57344-145-01

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 57344-145-01
Digits Only 5734414501
Product NDC 57344-145
Description

1 BOTTLE, PLASTIC in 1 CARTON (57344-145-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2012-04-01
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": "37ca1c84-c35c-0cfa-e063-6294a90a70bd", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["5ea3217d-845d-4781-b849-6b00babdc214"], "manufacturer_name": ["AAA Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57344-145-01)  / 24 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57344-145-01", "marketing_start_date": "20120401"}], "brand_name": "NAPROXEN SODIUM", "product_id": "57344-145_37ca1c84-c35c-0cfa-e063-6294a90a70bd", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "57344-145", "generic_name": "NAPROXEN SODIUM", "labeler_name": "AAA Pharmaceutical, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NAPROXEN SODIUM", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20120401", "listing_expiration_date": "20261231"}