Package 70518-3779-0

Brand: diclofenac sodium

Generic: diclofenac sodium topical
NDC Package

Package 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
Marketed Since 2023-07-07
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"}