Package 71921-400-10

Brand: dorzolamide hydrochloride ophthalmic

Generic: dorzolamide hydrochloride ophthalmic
NDC Package

Package Facts

Identity

Package NDC 71921-400-10
Digits Only 7192140010
Product NDC 71921-400
Description

10 mL in 1 BOTTLE (71921-400-10)

Marketing

Marketing Status
Marketed Since 2025-05-07
Brand dorzolamide hydrochloride ophthalmic
Generic dorzolamide hydrochloride ophthalmic
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "e4e6a5a8-f7be-4424-83f2-d6bb4d57443e", "openfda": {"upc": ["0371921400102"], "unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["e4e6a5a8-f7be-4424-83f2-d6bb4d57443e"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE (71921-400-10)", "package_ndc": "71921-400-10", "marketing_start_date": "20250507"}], "brand_name": "Dorzolamide Hydrochloride Ophthalmic", "product_id": "71921-400_e4e6a5a8-f7be-4424-83f2-d6bb4d57443e", "dosage_form": "SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "71921-400", "generic_name": "Dorzolamide Hydrochloride Ophthalmic", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dorzolamide Hydrochloride Ophthalmic", "active_ingredients": [{"name": "DORZOLAMIDE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA202053", "marketing_category": "ANDA", "marketing_start_date": "20250507", "listing_expiration_date": "20261231"}