Package 51655-176-84

{"route": ["ORAL"], "spl_id": "48c42861-3d59-b822-e063-6394a90acaf9", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["c16e7e43-3869-9fef-e053-2995a90a1fdb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-26)", "package_ndc": "51655-176-26", "marketing_start_date": "20230717"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-52)", "package_ndc": "51655-176-52", "marketing_start_date": "20220714"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-176-84)", "package_ndc": "51655-176-84", "marketing_start_date": "20200929"}], "brand_name": "Diclofenac Sodium Delayed Release", "product_id": "51655-176_48c42861-3d59-b822-e063-6394a90acaf9", "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": "51655-176", "generic_name": "Diclofenac Sodium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "20200929", "listing_expiration_date": "20271231"}