Package 50742-278-01
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
50742-278-01
Digits Only
5074227801
Product NDC
50742-278
Description
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-278-01)
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": "37537219-52df-4924-8bae-4188c8eb922b", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["1a237198-ca24-4159-b570-b5a23c8e91b0"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50742-278-01)", "package_ndc": "50742-278-01", "marketing_start_date": "20220926"}], "brand_name": "Diclofenac sodium", "product_id": "50742-278_37537219-52df-4924-8bae-4188c8eb922b", "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": "50742-278", "generic_name": "diclofenac sodium", "labeler_name": "Ingenus Pharmaceuticals, LLC", "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": "20220926", "listing_expiration_date": "20271231"}