Package 50090-1912-0
Brand: prednisolone acetate
Generic: prednisolone acetatePackage Facts
Identity
Package NDC
50090-1912-0
Digits Only
5009019120
Product NDC
50090-1912
Description
1 BOTTLE, DROPPER in 1 CARTON (50090-1912-0) / 10 mL in 1 BOTTLE, DROPPER
Marketing
Marketing Status
Brand
prednisolone acetate
Generic
prednisolone acetate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "b8aba180-92d1-4759-b2eb-f02bc95a2b8f", "openfda": {"unii": ["8B2807733D"], "rxcui": ["1376336"], "spl_set_id": ["388abc87-cd5a-4e88-8675-7bf0c5ce7af5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (50090-1912-0) / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "50090-1912-0", "marketing_start_date": "20150701"}], "brand_name": "PREDNISOLONE ACETATE", "product_id": "50090-1912_b8aba180-92d1-4759-b2eb-f02bc95a2b8f", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-1912", "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": "NDA017011", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19970819", "listing_expiration_date": "20261231"}