Package 50090-1912-0

Brand: prednisolone acetate

Generic: prednisolone acetate
NDC Package

Package 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
Marketed Since 2015-07-01
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"}