Package 74157-016-60

Brand: diclofenac potassium

Generic: diclofenac potassium, film coated
NDC Package

Package Facts

Identity

Package NDC 74157-016-60
Digits Only 7415701660
Product NDC 74157-016
Description

60 TABLET in 1 BOTTLE (74157-016-60)

Marketing

Marketing Status
Marketed Since 2024-10-01
Brand diclofenac potassium
Generic diclofenac potassium, film coated
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46416667-2723-f845-e063-6294a90a6748", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["857702"], "spl_set_id": ["6c703075-b9a3-42de-87f6-fd1e1ef4b2e3"], "manufacturer_name": ["INA Pharmaceutics Inc,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (74157-016-60)", "package_ndc": "74157-016-60", "marketing_start_date": "20241001"}], "brand_name": "DICLOFENAC POTASSIUM", "product_id": "74157-016_46416667-2723-f845-e063-6294a90a6748", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "74157-016", "generic_name": "diclofenac potassium, film coated", "labeler_name": "INA Pharmaceutics Inc,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DICLOFENAC POTASSIUM", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA215787", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}