Package 0527-5160-82
Brand: mycophenolate mofetil
Generic: mycophenolate mofetilPackage Facts
Identity
Package NDC
0527-5160-82
Digits Only
0527516082
Product NDC
0527-5160
Description
1 BOTTLE, PLASTIC in 1 CARTON (0527-5160-82) / 225 mL in 1 BOTTLE, PLASTIC
Marketing
Marketing Status
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": "6cb7ed46-e457-4e92-8a15-e771e3dca2d5", "openfda": {"unii": ["9242ECW6R0"], "rxcui": ["311880"], "spl_set_id": ["24c0b94a-c141-44b6-a6f0-ade1669b254c"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0527-5160-82) / 225 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0527-5160-82", "marketing_start_date": "20210729"}], "brand_name": "Mycophenolate Mofetil", "product_id": "0527-5160_6cb7ed46-e457-4e92-8a15-e771e3dca2d5", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Antimetabolite Immunosuppressant [EPC]"], "product_ndc": "0527-5160", "generic_name": "Mycophenolate Mofetil", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycophenolate Mofetil", "active_ingredients": [{"name": "MYCOPHENOLATE MOFETIL", "strength": "200 mg/mL"}], "application_number": "ANDA214525", "marketing_category": "ANDA", "marketing_start_date": "20210729", "listing_expiration_date": "20261231"}