Package 0832-6054-05

Brand: difluprednate

Generic: difluprednate
NDC Package

Package Facts

Identity

Package NDC 0832-6054-05
Digits Only 0832605405
Product NDC 0832-6054
Description

1 BOTTLE in 1 CARTON (0832-6054-05) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-08-21
Brand difluprednate
Generic difluprednate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "4af796ab-94c3-c22a-e063-6294a90abcb3", "openfda": {"unii": ["S8A06QG2QE"], "rxcui": ["804544"], "spl_set_id": ["ce8c1d56-771e-45da-8a19-5f881f993738"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0832-6054-05)  / 5 mL in 1 BOTTLE", "package_ndc": "0832-6054-05", "marketing_start_date": "20250821"}], "brand_name": "Difluprednate", "product_id": "0832-6054_4af796ab-94c3-c22a-e063-6294a90abcb3", "dosage_form": "EMULSION", "product_ndc": "0832-6054", "generic_name": "Difluprednate", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Difluprednate", "active_ingredients": [{"name": "DIFLUPREDNATE", "strength": ".5 mg/mL"}], "application_number": "ANDA218191", "marketing_category": "ANDA", "marketing_start_date": "20250221", "listing_expiration_date": "20271231"}