Package 67877-230-22

Brand: mycophenolate mofetil

Generic: mycophenolate mofetil
NDC Package

Package Facts

Identity

Package NDC 67877-230-22
Digits Only 6787723022
Product NDC 67877-230
Product ID 67877-230_d57b5ef3-52b0-473c-aa54-3208566e5909
Description

1 BOTTLE, PLASTIC in 1 CARTON (67877-230-22) / 225 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2014-11-17
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": "d57b5ef3-52b0-473c-aa54-3208566e5909", "openfda": {"upc": ["0367877230221"], "unii": ["9242ECW6R0"], "rxcui": ["311880"], "spl_set_id": ["21ff53b0-b4ba-4473-91e4-76ef41681064"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (67877-230-22)  / 225 mL in 1 BOTTLE, PLASTIC", "package_ndc": "67877-230-22", "marketing_start_date": "20141117"}], "brand_name": "Mycophenolate mofetil", "product_id": "67877-230_d57b5ef3-52b0-473c-aa54-3208566e5909", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "67877-230", "generic_name": "Mycophenolate mofetil", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "ANDA203005", "marketing_category": "ANDA", "marketing_start_date": "20141117", "listing_expiration_date": "20261231"}