dorzolamide hydrochloride
Generic: dorzolamide hydrochloride
Labeler: fosun pharma usa incDrug Facts
Product Profile
Brand Name
dorzolamide hydrochloride
Generic Name
dorzolamide hydrochloride
Labeler
fosun pharma usa inc
Dosage Form
SOLUTION
Routes
Active Ingredients
dorzolamide hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72266-197
Product ID
72266-197_3fb5657e-e6e3-066b-e063-6294a90a67ab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215660
Listing Expiration
2026-12-31
Marketing Start
2023-01-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72266197
Hyphenated Format
72266-197
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dorzolamide hydrochloride (source: ndc)
Generic Name
dorzolamide hydrochloride (source: ndc)
Application Number
ANDA215660 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (72266-197-01) / 10 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
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"}