Package 50090-0559-0

Brand: prednisolone acetate

Generic: prednisolone acetate
NDC Package

Package Facts

Identity

Package NDC 50090-0559-0
Digits Only 5009005590
Product NDC 50090-0559
Product ID 50090-0559_54821cc4-1238-4ab7-926f-4e6a185d55e5
Description

1 BOTTLE, PLASTIC in 1 CARTON (50090-0559-0) / 10 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2016-06-29
Brand prednisolone acetate
Generic prednisolone acetate
Sample Package No

Linked Drug Pages (1)

Prednisolone Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "54821cc4-1238-4ab7-926f-4e6a185d55e5", "openfda": {"unii": ["8B2807733D"], "rxcui": ["1376336"], "spl_set_id": ["b1d30a4f-4941-45a5-bd24-fea07f1bfc87"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50090-0559-0)  / 10 mL in 1 BOTTLE, PLASTIC", "package_ndc": "50090-0559-0", "marketing_start_date": "20160629"}], "brand_name": "Prednisolone Acetate", "product_id": "50090-0559_54821cc4-1238-4ab7-926f-4e6a185d55e5", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-0559", "generic_name": "Prednisolone Acetate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Acetate", "active_ingredients": [{"name": "PREDNISOLONE ACETATE", "strength": "10 mg/mL"}], "application_number": "NDA017469", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19941215", "listing_expiration_date": "20261231"}