Package 70069-501-01
Brand: dorzolamide hydrochloride
Generic: dorzolamide hydrochloridePackage Facts
Identity
Package NDC
70069-501-01
Digits Only
7006950101
Product NDC
70069-501
Description
1 BOTTLE in 1 CARTON (70069-501-01) / 10 mL in 1 BOTTLE
Marketing
Marketing Status
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": "599cbb55-78b6-467b-8762-fe20c11b013e", "openfda": {"upc": ["0370069501016"], "unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["0832960f-0a6f-4fd1-bf55-be9bebde53bd"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-501-01) / 10 mL in 1 BOTTLE", "package_ndc": "70069-501-01", "marketing_start_date": "20250212"}], "brand_name": "Dorzolamide Hydrochloride", "product_id": "70069-501_599cbb55-78b6-467b-8762-fe20c11b013e", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "70069-501", "generic_name": "Dorzolamide Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dorzolamide Hydrochloride", "active_ingredients": [{"name": "DORZOLAMIDE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA215004", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}