Package 42799-953-01
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
42799-953-01
Digits Only
4279995301
Product NDC
42799-953
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42799-953-01)
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": "50827dab-3a98-4af3-ba36-3afcd814c6e3", "openfda": {"upc": ["0342799953014"], "unii": ["QTG126297Q"], "rxcui": ["855657"], "spl_set_id": ["bd25a2b1-a4d5-4893-97d1-efdcd414a97d"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42799-953-01)", "package_ndc": "42799-953-01", "marketing_start_date": "20230614"}], "brand_name": "Diclofenac Sodium", "product_id": "42799-953_50827dab-3a98-4af3-ba36-3afcd814c6e3", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "42799-953", "generic_name": "Diclofenac Sodium", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "100 mg/1"}], "application_number": "ANDA076201", "marketing_category": "ANDA", "marketing_start_date": "20021106", "listing_expiration_date": "20271231"}