Package 70518-1829-3

Brand: sulfasalazine

Generic: sulfasalazine
NDC Package

Package Facts

Identity

Package NDC 70518-1829-3
Digits Only 7051818293
Product NDC 70518-1829
Description

30 TABLET in 1 BLISTER PACK (70518-1829-3)

Marketing

Marketing Status
Marketed Since 2021-10-29
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": "4976ef9d-bb2f-1498-e063-6294a90a81d2", "openfda": {"nui": ["N0000175781", "M0000971"], "unii": ["3XC8GUZ6CB"], "rxcui": ["198232"], "spl_set_id": ["88441a9f-b4f9-455d-a355-46fb30699a7b"], "pharm_class_cs": ["Aminosalicylic Acids [CS]"], "pharm_class_epc": ["Aminosalicylate [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1829-3)", "package_ndc": "70518-1829-3", "marketing_start_date": "20211029"}], "brand_name": "Sulfasalazine", "product_id": "70518-1829_4976ef9d-bb2f-1498-e063-6294a90a81d2", "dosage_form": "TABLET", "pharm_class": ["Aminosalicylate [EPC]", "Aminosalicylic Acids [CS]"], "product_ndc": "70518-1829", "generic_name": "Sulfasalazine", "labeler_name": "REMEDYREPACK 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": "20190128", "listing_expiration_date": "20271231"}