Package 68001-280-00
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
68001-280-00
Digits Only
6800128000
Product NDC
68001-280
Description
100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-00)
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": "411b49de-cfcc-2b9f-e063-6394a90a06b7", "openfda": {"upc": ["0368001280006", "0368001281003"], "unii": ["QTG126297Q"], "rxcui": ["855664", "855906", "855926"], "spl_set_id": ["feb1541a-de83-47dd-be03-c43376527318"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-00)", "package_ndc": "68001-280-00", "marketing_start_date": "20151221"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-06)", "package_ndc": "68001-280-06", "marketing_start_date": "20151221"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-08)", "package_ndc": "68001-280-08", "marketing_start_date": "20151221"}], "brand_name": "Diclofenac Sodium", "product_id": "68001-280_411b49de-cfcc-2b9f-e063-6394a90a06b7", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68001-280", "generic_name": "Diclofenac Sodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA090066", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}