Package 69315-329-05

Brand: difluprednate

Generic: difluprednate
NDC Package

Package Facts

Identity

Package NDC 69315-329-05
Digits Only 6931532905
Product NDC 69315-329
Product ID 69315-329_3dd0b742-d0d7-4922-8c9d-01293432b710
Description

1 BOTTLE in 1 CARTON (69315-329-05) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-02-18
Brand difluprednate
Generic difluprednate
Sample Package No

Linked Drug Pages (1)

DIFLUPREDNATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "3dd0b742-d0d7-4922-8c9d-01293432b710", "openfda": {"upc": ["0369315329054"], "unii": ["S8A06QG2QE"], "rxcui": ["804544"], "spl_set_id": ["054ca798-454a-41cc-9d08-97bb8bef5620"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69315-329-05)  / 5 mL in 1 BOTTLE", "package_ndc": "69315-329-05", "marketing_start_date": "20250218"}], "brand_name": "DIFLUPREDNATE", "product_id": "69315-329_3dd0b742-d0d7-4922-8c9d-01293432b710", "dosage_form": "EMULSION", "product_ndc": "69315-329", "generic_name": "DIFLUPREDNATE", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DIFLUPREDNATE", "active_ingredients": [{"name": "DIFLUPREDNATE", "strength": ".5 mg/mL"}], "application_number": "ANDA219441", "marketing_category": "ANDA", "marketing_start_date": "20250218", "listing_expiration_date": "20261231"}