Package 68001-612-00
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
68001-612-00
Digits Only
6800161200
Product NDC
68001-612
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68001-612-00)
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac sodium
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3427254e-c0d3-8413-e063-6394a90a766e", "openfda": {"upc": ["0368001612005"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["896e3f7d-88e6-4563-b879-a2757d19fd62"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68001-612-00)", "package_ndc": "68001-612-00", "marketing_start_date": "20240212"}], "brand_name": "Diclofenac sodium", "product_id": "68001-612_3427254e-c0d3-8413-e063-6394a90a766e", "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": "68001-612", "generic_name": "diclofenac sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA216275", "marketing_category": "ANDA", "marketing_start_date": "20240212", "listing_expiration_date": "20261231"}