Package 70882-128-30

{"route": ["ORAL"], "spl_id": "b30b3f90-b9d8-4110-b0a8-5c18b8969832", "openfda": {"upc": ["0370882128308"], "unii": ["QTG126297Q"], "rxcui": ["855926"], "spl_set_id": ["fd544812-d7a9-47c8-9148-bea26c8b66c7"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70882-128-30)", "package_ndc": "70882-128-30", "marketing_start_date": "19981113"}], "brand_name": "Diclofenac Sodium Delayed Release Delayed Release", "product_id": "70882-128_b30b3f90-b9d8-4110-b0a8-5c18b8969832", "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": "70882-128", "generic_name": "Diclofenac Sodium", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Sodium Delayed Release", "brand_name_suffix": "Delayed Release", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "75 mg/1"}], "application_number": "ANDA075185", "marketing_category": "ANDA", "marketing_start_date": "19981113", "listing_expiration_date": "20261231"}