Package 73352-086-30

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 73352-086-30
Digits Only 7335208630
Product NDC 73352-086
Product ID 73352-086_e1409a25-9dd7-4c50-ae45-7dbaee133125
Description

30 TABLET, COATED in 1 BOTTLE (73352-086-30)

Marketing

Marketing Status
Marketed Since 2023-02-17
Brand diclofenac potassium
Generic diclofenac potassium
Sample Package No

Linked Drug Pages (1)

Diclofenac Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e1409a25-9dd7-4c50-ae45-7dbaee133125", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["857702"], "spl_set_id": ["8fdb1036-c0d8-4288-ac37-6512b05672ef"], "manufacturer_name": ["Trifluent Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (73352-086-30)", "package_ndc": "73352-086-30", "marketing_start_date": "20230217"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (73352-086-60)", "package_ndc": "73352-086-60", "marketing_start_date": "20230925"}], "brand_name": "Diclofenac Potassium", "product_id": "73352-086_e1409a25-9dd7-4c50-ae45-7dbaee133125", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "73352-086", "generic_name": "diclofenac potassium", "labeler_name": "Trifluent Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA075229", "marketing_category": "ANDA", "marketing_start_date": "20230217", "listing_expiration_date": "20261231"}