Package 50090-7539-0

Brand: prednisolone acetate

Generic: prednisolone acetate
NDC Package

Package Facts

Identity

Package NDC 50090-7539-0
Digits Only 5009075390
Product NDC 50090-7539
Product ID 50090-7539_af502300-c29e-405b-bb6f-f125d432a2c1
Description

1 BOTTLE in 1 CARTON (50090-7539-0) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-04-22
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": "af502300-c29e-405b-bb6f-f125d432a2c1", "openfda": {"unii": ["8B2807733D"], "rxcui": ["1376336"], "spl_set_id": ["f0e1b691-73ff-49ee-8a3c-71769b284ab8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50090-7539-0)  / 5 mL in 1 BOTTLE", "package_ndc": "50090-7539-0", "marketing_start_date": "20250422"}], "brand_name": "PREDNISOLONE ACETATE", "product_id": "50090-7539_af502300-c29e-405b-bb6f-f125d432a2c1", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7539", "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": "ANDA216935", "marketing_category": "ANDA", "marketing_start_date": "20241011", "listing_expiration_date": "20271231"}