Package 50742-317-25

Brand: flunisolide

Generic: flunisolide
NDC Package

Package Facts

Identity

Package NDC 50742-317-25
Digits Only 5074231725
Product NDC 50742-317
Product ID 50742-317_139fb92c-bb10-4ee9-8572-679ac540aa27
Description

1 BOTTLE, PUMP in 1 CARTON (50742-317-25) / 25 mL in 1 BOTTLE, PUMP

Marketing

Marketing Status
Marketed Since 2022-06-23
Brand flunisolide
Generic flunisolide
Sample Package No

Linked Drug Pages (1)

Flunisolide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "139fb92c-bb10-4ee9-8572-679ac540aa27", "openfda": {"unii": ["QK4DYS664X"], "rxcui": ["1797863"], "spl_set_id": ["f39cae46-c68f-47ef-82f3-4fd3dd46c74c"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PUMP in 1 CARTON (50742-317-25)  / 25 mL in 1 BOTTLE, PUMP", "package_ndc": "50742-317-25", "marketing_start_date": "20220623"}], "brand_name": "Flunisolide", "product_id": "50742-317_139fb92c-bb10-4ee9-8572-679ac540aa27", "dosage_form": "SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50742-317", "generic_name": "Flunisolide", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flunisolide", "active_ingredients": [{"name": "FLUNISOLIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA207802", "marketing_category": "ANDA", "marketing_start_date": "20220623", "listing_expiration_date": "20261231"}