Package 70518-3779-0
Brand: diclofenac sodium
Generic: diclofenac sodium topicalPackage Facts
Identity
Package NDC
70518-3779-0
Digits Only
7051837790
Product NDC
70518-3779
Description
1 TUBE in 1 CARTON (70518-3779-0) / 100 g in 1 TUBE
Marketing
Marketing Status
Brand
diclofenac sodium
Generic
diclofenac sodium topical
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "44571ac5-48af-8546-e063-6294a90a515b", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855642"], "spl_set_id": ["cc8c3125-ee43-40bb-8500-339efa901b8c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70518-3779-0) / 100 g in 1 TUBE", "package_ndc": "70518-3779-0", "marketing_start_date": "20230707"}], "brand_name": "Diclofenac Sodium", "product_id": "70518-3779_44571ac5-48af-8546-e063-6294a90a515b", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70518-3779", "generic_name": "Diclofenac Sodium Topical", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "30 mg/g"}], "application_number": "ANDA212351", "marketing_category": "ANDA", "marketing_start_date": "20230707", "listing_expiration_date": "20261231"}