Package 72266-197-01

Brand: dorzolamide hydrochloride

Generic: dorzolamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72266-197-01
Digits Only 7226619701
Product NDC 72266-197
Description

1 BOTTLE in 1 CARTON (72266-197-01) / 10 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-01-23
Brand dorzolamide hydrochloride
Generic dorzolamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "3fb5657e-e6e3-066b-e063-6294a90a67ab", "openfda": {"unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["ef173b63-499f-301b-e053-2995a90a4771"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72266-197-01)  / 10 mL in 1 BOTTLE", "package_ndc": "72266-197-01", "marketing_start_date": "20230123"}], "brand_name": "Dorzolamide Hydrochloride", "product_id": "72266-197_3fb5657e-e6e3-066b-e063-6294a90a67ab", "dosage_form": "SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "72266-197", "generic_name": "Dorzolamide Hydrochloride", "labeler_name": "FOSUN PHARMA USA INC", "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": "20230123", "listing_expiration_date": "20261231"}