Package 42571-141-26

Brand: dorzolamide hydrochloride ophthalmic solution

Generic: dorzolamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42571-141-26
Digits Only 4257114126
Product NDC 42571-141
Description

1 BOTTLE in 1 CARTON (42571-141-26) / 10 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-11-11
Brand dorzolamide hydrochloride ophthalmic solution
Generic dorzolamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "2b30c4d1-0a5d-3ad8-e063-6394a90a4acb", "openfda": {"upc": ["0342571141264"], "unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["4698e4e1-c5f6-4db1-9328-74464a85afea"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (42571-141-26)  / 10 mL in 1 BOTTLE", "package_ndc": "42571-141-26", "marketing_start_date": "20191111"}], "brand_name": "Dorzolamide Hydrochloride Ophthalmic Solution", "product_id": "42571-141_2b30c4d1-0a5d-3ad8-e063-6394a90a4acb", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "42571-141", "generic_name": "Dorzolamide Hydrochloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dorzolamide Hydrochloride Ophthalmic Solution", "active_ingredients": [{"name": "DORZOLAMIDE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA204778", "marketing_category": "ANDA", "marketing_start_date": "20191111", "listing_expiration_date": "20261231"}