Package 72819-151-10

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 72819-151-10
Digits Only 7281915110
Product NDC 72819-151
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72819-151-10)

Marketing

Marketing Status
Marketed Since 2021-09-15
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": "2a824504-c49c-b0d3-e063-6294a90a973c", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["0d83cab3-c698-4763-9e77-27d72ba94e30"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72819-151-10)", "package_ndc": "72819-151-10", "marketing_start_date": "20210915"}], "brand_name": "Diclofenac Potassium", "product_id": "72819-151_2a824504-c49c-b0d3-e063-6294a90a973c", "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": "72819-151", "generic_name": "diclofenac potassium", "labeler_name": "Archis Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075463", "marketing_category": "ANDA", "marketing_start_date": "20210915", "listing_expiration_date": "20261231"}