Package 66758-086-75

Brand: durezol

Generic: difluprednate
NDC Package

Package Facts

Identity

Package NDC 66758-086-75
Digits Only 6675808675
Product NDC 66758-086
Product ID 66758-086_4dadac60-2b25-486b-b716-86516821678c
Description

1 BOTTLE in 1 CARTON (66758-086-75) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-12-06
Brand durezol
Generic difluprednate
Sample Package No

Linked Drug Pages (1)

DUREZOL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "4dadac60-2b25-486b-b716-86516821678c", "openfda": {"unii": ["S8A06QG2QE"], "rxcui": ["804544", "804547"], "spl_set_id": ["ea520a27-f569-4b31-8bad-a25ad54b2caa"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (66758-086-75)  / 5 mL in 1 BOTTLE", "package_ndc": "66758-086-75", "marketing_start_date": "20241206"}], "brand_name": "DUREZOL", "product_id": "66758-086_4dadac60-2b25-486b-b716-86516821678c", "dosage_form": "EMULSION", "product_ndc": "66758-086", "generic_name": "difluprednate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DUREZOL", "active_ingredients": [{"name": "DIFLUPREDNATE", "strength": ".5 mg/mL"}], "application_number": "NDA022212", "marketing_category": "NDA", "marketing_start_date": "20110125", "listing_expiration_date": "20261231"}