Package 43598-588-11

Brand: difluprednate ophthalmic emulsion

Generic: difluprednate ophthalmic
NDC Package

Package Facts

Identity

Package NDC 43598-588-11
Digits Only 4359858811
Product NDC 43598-588
Description

1 BOTTLE in 1 CARTON (43598-588-11) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-12-25
Brand difluprednate ophthalmic emulsion
Generic difluprednate ophthalmic
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "acd98bc6-dcd8-d0f5-9b9a-d2652e0c37c6", "openfda": {"unii": ["S8A06QG2QE"], "rxcui": ["804544"], "spl_set_id": ["12803630-3196-1b3e-28e4-a598a742ef1a"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-588-11)  / 5 mL in 1 BOTTLE", "package_ndc": "43598-588-11", "marketing_start_date": "20221225"}], "brand_name": "Difluprednate Ophthalmic Emulsion", "product_id": "43598-588_acd98bc6-dcd8-d0f5-9b9a-d2652e0c37c6", "dosage_form": "EMULSION", "product_ndc": "43598-588", "generic_name": "Difluprednate Ophthalmic", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Difluprednate Ophthalmic Emulsion", "active_ingredients": [{"name": "DIFLUPREDNATE", "strength": ".5 mg/mL"}], "application_number": "ANDA214894", "marketing_category": "ANDA", "marketing_start_date": "20221225", "listing_expiration_date": "20261231"}