Package 0480-9435-89

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 0480-9435-89
Digits Only 0480943589
Product NDC 0480-9435
Description

120 CAPSULE, LIQUID FILLED in 1 BOTTLE (0480-9435-89)

Marketing

Marketing Status
Marketed Since 2022-03-24
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": "40461510-7592-d588-e063-6394a90a8b9e", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["858342"], "spl_set_id": ["d9685883-9d0b-81da-e053-2a95a90ab8d8"], "manufacturer_name": ["TEVA PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE (0480-9435-89)", "package_ndc": "0480-9435-89", "marketing_start_date": "20220324"}], "brand_name": "Diclofenac potassium", "product_id": "0480-9435_40461510-7592-d588-e063-6394a90a8b9e", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0480-9435", "generic_name": "diclofenac potassium", "labeler_name": "TEVA PHARMACEUTICALS, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA204648", "marketing_category": "ANDA", "marketing_start_date": "20220324", "listing_expiration_date": "20261231"}