Package 25021-006-10

Brand: dorzolamide hydrochloride

Generic: dorzolamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-006-10
Digits Only 2502100610
Product NDC 25021-006
Product ID 25021-006_1a198736-860b-4ea2-a5db-e6ca487441bf
Description

1 BOTTLE in 1 CARTON (25021-006-10) / 10 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2026-01-15
Brand dorzolamide hydrochloride
Generic dorzolamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Dorzolamide Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "1a198736-860b-4ea2-a5db-e6ca487441bf", "openfda": {"unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["0246463c-6c24-4611-8e22-2d5254ace66a"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (25021-006-10)  / 10 mL in 1 BOTTLE", "package_ndc": "25021-006-10", "marketing_start_date": "20260115"}], "brand_name": "Dorzolamide Hydrochloride", "product_id": "25021-006_1a198736-860b-4ea2-a5db-e6ca487441bf", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "25021-006", "generic_name": "Dorzolamide Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dorzolamide Hydrochloride", "active_ingredients": [{"name": "DORZOLAMIDE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA215660", "marketing_category": "ANDA", "marketing_start_date": "20260115", "listing_expiration_date": "20271231"}