Package 70518-2707-2

{"route": ["ORAL"], "spl_id": "4a7e2225-0919-b83f-e063-6294a90afc10", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855906"], "spl_set_id": ["ddd2278b-70be-41ca-8a84-e3fe0f1a1561"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2707-2)", "package_ndc": "70518-2707-2", "marketing_start_date": "20211020"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2707-3)", "package_ndc": "70518-2707-3", "marketing_start_date": "20250811"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "70518-2707_4a7e2225-0919-b83f-e063-6294a90afc10", "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": "70518-2707", "generic_name": "Diclofenac Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20200423", "listing_expiration_date": "20271231"}