Package 68071-2223-7
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
68071-2223-7
Digits Only
6807122237
Product NDC
68071-2223
Description
7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-2223-7)
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d7609b9-edfe-178d-e063-6294a90a3626", "openfda": {"upc": ["0368071222371"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["abacf60f-0410-e6da-e053-2995a90a413c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-2223-7)", "package_ndc": "68071-2223-7", "marketing_start_date": "20200730"}], "brand_name": "Diclofenac Sodium", "product_id": "68071-2223_1d7609b9-edfe-178d-e063-6294a90a3626", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-2223", "generic_name": "Diclofenac Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA075492", "marketing_category": "ANDA", "marketing_start_date": "20000228", "listing_expiration_date": "20261231"}