dorzolamide hydrochloride

Generic: dorzolamide hydrochloride

Labeler: fosun pharma usa inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dorzolamide hydrochloride
Generic Name dorzolamide hydrochloride
Labeler fosun pharma usa inc
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

dorzolamide hydrochloride 20 mg/mL

Manufacturer
FOSUN PHARMA USA INC

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
carbonic anhydrase inhibitor [epc] carbonic anhydrase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266197
Hyphenated Format 72266-197

Supplemental Identifiers

RxCUI
310015
UNII
QZO5366EW7

Packaging Origin

Original Packager
true

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
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (72266-197-01) / 10 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

dorzolamide hydrochloride (20 mg/mL)

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"}