Package 50090-7647-0
Brand: diclofenac sodium
Generic: diclofenac sodiumPackage Facts
Identity
Package NDC
50090-7647-0
Digits Only
5009076470
Product NDC
50090-7647
Description
90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7647-0)
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": "6b9a6a44-9dd6-44a3-a9dd-037469d78110", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["4c5b722e-0d1a-48e9-87c8-9b370b8ced46"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7647-0)", "package_ndc": "50090-7647-0", "marketing_start_date": "20250903"}], "brand_name": "Diclofenac Sodium", "product_id": "50090-7647_6b9a6a44-9dd6-44a3-a9dd-037469d78110", "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": "50090-7647", "generic_name": "Diclofenac Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA216548", "marketing_category": "ANDA", "marketing_start_date": "20250423", "listing_expiration_date": "20261231"}