Package 50742-279-01

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 50742-279-01
Digits Only 5074227901
Product NDC 50742-279
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-279-01)

Marketing

Marketing Status
Marketed Since 2021-10-11
Brand diclofenac potassium
Generic diclofenac potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "921cc254-7a32-43b8-a2c8-298f39b32226", "openfda": {"upc": ["0350742279012"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["6926444f-0dca-4aeb-812e-755a83b149f4"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-279-01)", "package_ndc": "50742-279-01", "marketing_start_date": "20211011"}], "brand_name": "Diclofenac Potassium", "product_id": "50742-279_921cc254-7a32-43b8-a2c8-298f39b32226", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50742-279", "generic_name": "diclofenac potassium", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215585", "marketing_category": "ANDA", "marketing_start_date": "20211011", "listing_expiration_date": "20261231"}