Package 61314-019-10

Brand: dorzolamide hydrochloride

Generic: dorzolamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 61314-019-10
Digits Only 6131401910
Product NDC 61314-019
Product ID 61314-019_764fec18-11c4-4320-a834-83c80c7040d2
Description

10 mL in 1 BOTTLE (61314-019-10)

Marketing

Marketing Status
Marketed Since 2009-06-01
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": "764fec18-11c4-4320-a834-83c80c7040d2", "openfda": {"unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["29157995-fa61-4425-86a5-5bd0e4718cd8"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE (61314-019-10)", "package_ndc": "61314-019-10", "marketing_start_date": "20090601"}], "brand_name": "DORZOLAMIDE HYDROCHLORIDE", "product_id": "61314-019_764fec18-11c4-4320-a834-83c80c7040d2", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "61314-019", "generic_name": "dorzolamide hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DORZOLAMIDE HYDROCHLORIDE", "active_ingredients": [{"name": "DORZOLAMIDE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA078981", "marketing_category": "ANDA", "marketing_start_date": "20090601", "listing_expiration_date": "20261231"}