Package 82293-013-10

Brand: mycophenolic acid

Generic: mycophenolic acid
NDC Package

Package Facts

Identity

Package NDC 82293-013-10
Digits Only 8229301310
Product NDC 82293-013
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (82293-013-10)

Marketing

Marketing Status
Marketed Since 2024-09-01
Brand mycophenolic acid
Generic mycophenolic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f0154d5-686f-170e-e063-6394a90a67e6", "openfda": {"unii": ["WX877SQI1G"], "rxcui": ["485020", "485023"], "spl_set_id": ["cbc3e916-09e2-4e6e-9e5e-98375f5e6d41"], "manufacturer_name": ["Novugen Pharma (USA) LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (82293-013-10)", "package_ndc": "82293-013-10", "marketing_start_date": "20240901"}], "brand_name": "Mycophenolic Acid", "product_id": "82293-013_1f0154d5-686f-170e-e063-6394a90a67e6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "82293-013", "generic_name": "Mycophenolic Acid", "labeler_name": "Novugen Pharma (USA) LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolic Acid", "active_ingredients": [{"name": "MYCOPHENOLATE SODIUM", "strength": "360 mg/1"}], "application_number": "ANDA216637", "marketing_category": "ANDA", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}