Package 42291-042-01

Brand: diclofenac potassium

Generic: diclofenac potassium
NDC Package

Package Facts

Identity

Package NDC 42291-042-01
Digits Only 4229104201
Product NDC 42291-042
Product ID 42291-042_484c1058-0a5d-1582-e063-6394a90a2985
Description

100 TABLET, FILM COATED in 1 BOTTLE (42291-042-01)

Marketing

Marketing Status
Marketed Since 2024-09-11
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": "484c1058-0a5d-1582-e063-6394a90a2985", "openfda": {"upc": ["0342291042018"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["21dc9953-4e6d-50f0-e063-6294a90ac4ef"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42291-042-01)", "package_ndc": "42291-042-01", "marketing_start_date": "20240911"}], "brand_name": "Diclofenac Potassium", "product_id": "42291-042_484c1058-0a5d-1582-e063-6394a90a2985", "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": "42291-042", "generic_name": "diclofenac potassium", "labeler_name": "AvKARE", "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": "20240911", "listing_expiration_date": "20271231"}