Package 68071-3451-3

Brand: diclofenac potassium

Generic: diclofenac potassium tablets
NDC Package

Package Facts

Identity

Package NDC 68071-3451-3
Digits Only 6807134513
Product NDC 68071-3451
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3451-3)

Marketing

Marketing Status
Marketed Since 2023-07-05
Brand diclofenac potassium
Generic diclofenac potassium tablets
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d68439e-17d1-b835-e063-6294a90a4737", "openfda": {"upc": ["0368071345131"], "unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["ffc41543-a353-cade-e053-6294a90a99fb"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3451-3)", "package_ndc": "68071-3451-3", "marketing_start_date": "20230705"}], "brand_name": "Diclofenac Potassium", "product_id": "68071-3451_2d68439e-17d1-b835-e063-6294a90a4737", "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": "68071-3451", "generic_name": "Diclofenac Potassium Tablets", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215750", "marketing_category": "ANDA", "marketing_start_date": "20220512", "listing_expiration_date": "20261231"}