Package 0013-0102-50

{"route": ["ORAL"], "spl_id": "e085ce86-abc0-4032-a3c9-ca89bae152d9", "openfda": {"nui": ["N0000175781", "M0000971"], "unii": ["3XC8GUZ6CB"], "rxcui": ["313142", "724154"], "spl_set_id": ["b9ef541a-93c8-4428-ba45-398aa0b327d1"], "pharm_class_cs": ["Aminosalicylic Acids [CS]"], "pharm_class_epc": ["Aminosalicylate [EPC]"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0013-0102-50)  / 100 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "0013-0102-50", "marketing_start_date": "20200707"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0013-0102-60)  / 300 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "0013-0102-60", "marketing_start_date": "20210215"}], "brand_name": "Azulfidine EN-tabs", "product_id": "0013-0102_e085ce86-abc0-4032-a3c9-ca89bae152d9", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Aminosalicylate [EPC]", "Aminosalicylic Acids [CS]"], "product_ndc": "0013-0102", "generic_name": "Sulfasalazine", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azulfidine", "brand_name_suffix": "EN-tabs", "active_ingredients": [{"name": "SULFASALAZINE", "strength": "500 mg/1"}], "application_number": "NDA007073", "marketing_category": "NDA", "marketing_start_date": "19500620", "listing_expiration_date": "20261231"}