Package 24208-715-10

Brand: prednisolone sodium phosphate

Generic: prednisolone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 24208-715-10
Digits Only 2420871510
Product NDC 24208-715
Description

1 BOTTLE, DROPPER in 1 CARTON (24208-715-10) / 10 mL in 1 BOTTLE, DROPPER

Marketing

Marketing Status
Marketed Since 1999-07-29
Brand prednisolone sodium phosphate
Generic prednisolone sodium phosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "87bea906-f7cf-4987-abb2-02981b5ea0e2", "openfda": {"unii": ["IV021NXA9J"], "rxcui": ["314165"], "spl_set_id": ["8a7f0f2a-3a48-4488-89cd-3e91c3b1365f"], "manufacturer_name": ["Bausch & Lomb Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (24208-715-10)  / 10 mL in 1 BOTTLE, DROPPER", "package_ndc": "24208-715-10", "marketing_start_date": "19990729"}], "brand_name": "PREDNISOLONE SODIUM PHOSPHATE", "product_id": "24208-715_87bea906-f7cf-4987-abb2-02981b5ea0e2", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "24208-715", "generic_name": "PREDNISOLONE SODIUM PHOSPHATE", "labeler_name": "Bausch & Lomb Incorporated", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISOLONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "PREDNISOLONE SODIUM PHOSPHATE", "strength": "10 mg/mL"}], "application_number": "ANDA040070", "marketing_category": "ANDA", "marketing_start_date": "19940729", "listing_expiration_date": "20261231"}