Package 48201-007-24

Brand: calmadol pain reliever

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 48201-007-24
Digits Only 4820100724
Product NDC 48201-007
Description

1 PACKET in 1 BOX (48201-007-24) / 24 TABLET in 1 PACKET

Marketing

Marketing Status
Marketed Since 2015-03-31
Brand calmadol pain reliever
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4240708f-eaa2-9c13-e063-6294a90ab632", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["8edec8d1-a323-436b-8329-c327438516e3"], "manufacturer_name": ["GRANDALL DISTRIBUTING, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 PACKET in 1 BOX (48201-007-24)  / 24 TABLET in 1 PACKET", "package_ndc": "48201-007-24", "marketing_start_date": "20150331"}], "brand_name": "CALMADOL PAIN RELIEVER", "product_id": "48201-007_4240708f-eaa2-9c13-e063-6294a90ab632", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "48201-007", "generic_name": "Naproxen Sodium", "labeler_name": "GRANDALL DISTRIBUTING, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CALMADOL PAIN RELIEVER", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}