Package 72819-156-08

Brand: mycophenolic acid

Generic: mycophenilic acid
NDC Package

Package Facts

Identity

Package NDC 72819-156-08
Digits Only 7281915608
Product NDC 72819-156
Description

120 TABLET, DELAYED RELEASE in 1 BOTTLE (72819-156-08)

Marketing

Marketing Status
Marketed Since 2022-02-21
Brand mycophenolic acid
Generic mycophenilic acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "471a0acf-310d-7b67-e063-6294a90adb0e", "openfda": {"nui": ["N0000175613"], "upc": ["0378819155021"], "unii": ["HU9DX48N0T"], "rxcui": ["485020", "485023"], "spl_set_id": ["30cb1078-929b-4c0f-be1d-49ef352dfab9"], "pharm_class_epc": ["Antimetabolite Immunosuppressant [EPC]"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (72819-156-08)", "package_ndc": "72819-156-08", "marketing_start_date": "20220221"}], "brand_name": "Mycophenolic Acid", "product_id": "72819-156_471a0acf-310d-7b67-e063-6294a90adb0e", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "72819-156", "generic_name": "mycophenilic acid", "labeler_name": "Archis Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolic Acid", "active_ingredients": [{"name": "MYCOPHENOLIC ACID", "strength": "360 mg/1"}], "application_number": "ANDA091248", "marketing_category": "ANDA", "marketing_start_date": "20220221", "listing_expiration_date": "20261231"}