Package 0781-6000-78

Brand: difluprednate ophthalmic

Generic: difluprednate ophthalmic
NDC Package

Package Facts

Identity

Package NDC 0781-6000-78
Digits Only 0781600078
Product NDC 0781-6000
Product ID 0781-6000_6ae7a5b2-4844-4a63-a95e-8dd76c1e3653
Description

1 BOTTLE in 1 CARTON (0781-6000-78) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2021-09-15
Brand difluprednate ophthalmic
Generic difluprednate ophthalmic
Sample Package No

Linked Drug Pages (1)

Difluprednate Ophthalmic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "6ae7a5b2-4844-4a63-a95e-8dd76c1e3653", "openfda": {"upc": ["0307816000782"], "unii": ["S8A06QG2QE"], "rxcui": ["804544"], "spl_set_id": ["0f60b857-7898-4a9e-935c-a9ddf0eb9194"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0781-6000-78)  / 5 mL in 1 BOTTLE", "package_ndc": "0781-6000-78", "marketing_start_date": "20210915"}], "brand_name": "Difluprednate Ophthalmic", "product_id": "0781-6000_6ae7a5b2-4844-4a63-a95e-8dd76c1e3653", "dosage_form": "EMULSION", "product_ndc": "0781-6000", "generic_name": "Difluprednate Ophthalmic", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Difluprednate Ophthalmic", "active_ingredients": [{"name": "DIFLUPREDNATE", "strength": ".5 mg/mL"}], "application_number": "NDA022212", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20130515", "listing_expiration_date": "20261231"}