Package 59762-0104-5

Brand: sulfasalazine

Generic: sulfasalazine
NDC Package

Package Facts

Identity

Package NDC 59762-0104-5
Digits Only 5976201045
Product NDC 59762-0104
Description

1 BOTTLE in 1 CARTON (59762-0104-5) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-03-23
Brand sulfasalazine
Generic sulfasalazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d2a8dbd7-49db-4839-a5ee-0cbb39ae17ea", "openfda": {"nui": ["N0000175781", "M0000971"], "upc": ["0359762010414"], "unii": ["3XC8GUZ6CB"], "rxcui": ["313142"], "spl_set_id": ["257cee60-b68f-4c2b-b57d-8e4d73d17e09"], "pharm_class_cs": ["Aminosalicylic Acids [CS]"], "pharm_class_epc": ["Aminosalicylate [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59762-0104-5)  / 100 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "59762-0104-5", "marketing_start_date": "20200323"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (59762-0104-6)  / 300 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "59762-0104-6", "marketing_start_date": "20200406"}], "brand_name": "Sulfasalazine", "product_id": "59762-0104_d2a8dbd7-49db-4839-a5ee-0cbb39ae17ea", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Aminosalicylate [EPC]", "Aminosalicylic Acids [CS]"], "product_ndc": "59762-0104", "generic_name": "Sulfasalazine", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulfasalazine", "active_ingredients": [{"name": "SULFASALAZINE", "strength": "500 mg/1"}], "application_number": "NDA007073", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20050505", "listing_expiration_date": "20261231"}