Package 59651-638-01

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 59651-638-01
Digits Only 5965163801
Product NDC 59651-638
Description

100 TABLET, FILM COATED in 1 BOTTLE (59651-638-01)

Marketing

Marketing Status
Marketed Since 2024-02-20
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "abdd39b5-dac9-4e5c-9722-17473947909d", "openfda": {"upc": ["0359651638019"], "unii": ["9242ECW6R0"], "rxcui": ["200060"], "spl_set_id": ["8faf357b-99a1-440b-8eac-8545cb19a69c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-638-01)", "package_ndc": "59651-638-01", "marketing_start_date": "20240220"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-638-05)", "package_ndc": "59651-638-05", "marketing_start_date": "20240220"}], "brand_name": "Mycophenolate Mofetil", "product_id": "59651-638_abdd39b5-dac9-4e5c-9722-17473947909d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "59651-638", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "500 mg/1"}], "application_number": "ANDA217937", "marketing_category": "ANDA", "marketing_start_date": "20240220", "listing_expiration_date": "20261231"}