Package 70512-784-60

Brand: diclofenac sodium

Generic: diclofenac sodium
NDC Package

Package Facts

Identity

Package NDC 70512-784-60
Digits Only 7051278460
Product NDC 70512-784
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (70512-784-60)

Marketing

Marketing Status
Marketed Since 2025-11-14
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": "43cedf6d-7cca-c35c-e063-6294a90afd04", "openfda": {"upc": ["0370512784607"], "unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["b8072af2-9940-4827-9fbd-de46ad8bf929"], "manufacturer_name": ["SOLA Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (70512-784-60)", "package_ndc": "70512-784-60", "marketing_start_date": "20251114"}], "brand_name": "Diclofenac Sodium", "product_id": "70512-784_43cedf6d-7cca-c35c-e063-6294a90afd04", "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": "70512-784", "generic_name": "Diclofenac Sodium", "labeler_name": "SOLA Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20251114", "listing_expiration_date": "20261231"}