Package 0093-0948-01

{"route": ["ORAL"], "spl_id": "b9f656e7-0a32-460d-9c86-8065a7f4b108", "openfda": {"unii": ["L4D5UA6CB4"], "rxcui": ["855942"], "spl_set_id": ["77b60a0c-e49a-4ad4-abb1-b662c24ab782"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0948-01)", "package_ndc": "0093-0948-01", "marketing_start_date": "19980811"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-0948-05)", "package_ndc": "0093-0948-05", "marketing_start_date": "19980811"}], "brand_name": "Diclofenac Potassium", "product_id": "0093-0948_b9f656e7-0a32-460d-9c86-8065a7f4b108", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0093-0948", "generic_name": "Diclofenac Potassium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diclofenac Potassium", "active_ingredients": [{"name": "DICLOFENAC POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA075219", "marketing_category": "ANDA", "marketing_start_date": "19980811", "listing_expiration_date": "20261231"}