Package 66689-307-08

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 66689-307-08
Digits Only 6668930708
Product NDC 66689-307
Product ID 66689-307_1b2ac486-8e83-4fcf-998f-8e4f828cc406
Description

1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08) / 250 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2019-02-15
Brand mycophenolate mofetil
Generic mycophenolate mofetil
Sample Package No

Linked Drug Pages (1)

Mycophenolate Mofetil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b2ac486-8e83-4fcf-998f-8e4f828cc406", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311880"], "spl_set_id": ["175d8b87-e06a-4c9e-b3de-378114b52274"], "manufacturer_name": ["VistaPharm, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (66689-307-08)  / 250 mL in 1 BOTTLE, PLASTIC", "package_ndc": "66689-307-08", "marketing_start_date": "20190215"}], "brand_name": "Mycophenolate Mofetil", "product_id": "66689-307_1b2ac486-8e83-4fcf-998f-8e4f828cc406", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "66689-307", "generic_name": "Mycophenolate Mofetil", "labeler_name": "VistaPharm, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "ANDA210370", "marketing_category": "ANDA", "marketing_start_date": "20190215", "listing_expiration_date": "20261231"}