Package 46708-750-05

Brand: difluprednate

Generic: difluprednate ophthalmic
NDC Package

Package Facts

Identity

Package NDC 46708-750-05
Digits Only 4670875005
Product NDC 46708-750
Description

1 BOTTLE in 1 CARTON (46708-750-05) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2026-01-26
Brand difluprednate
Generic difluprednate ophthalmic
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "71121026-1496-4154-b61b-9afe9b62bf2a", "openfda": {"unii": ["S8A06QG2QE"], "rxcui": ["804544"], "spl_set_id": ["71121026-1496-4154-b61b-9afe9b62bf2a"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46708-750-05)  / 5 mL in 1 BOTTLE", "package_ndc": "46708-750-05", "marketing_start_date": "20260126"}], "brand_name": "Difluprednate", "product_id": "46708-750_71121026-1496-4154-b61b-9afe9b62bf2a", "dosage_form": "EMULSION", "product_ndc": "46708-750", "generic_name": "difluprednate ophthalmic", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Difluprednate", "active_ingredients": [{"name": "DIFLUPREDNATE", "strength": ".5 mg/mL"}], "application_number": "ANDA213774", "marketing_category": "ANDA", "marketing_start_date": "20260126", "listing_expiration_date": "20271231"}