dorzolamide hydrochloride
Generic: dorzolamide hydrochloride
Labeler: alembic pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
dorzolamide hydrochloride
Generic Name
dorzolamide hydrochloride
Labeler
alembic pharmaceuticals limited
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
dorzolamide hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
46708-519
Product ID
46708-519_64e77f0a-fff5-4e24-9af2-38a14b9a4ef9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212639
Listing Expiration
2026-12-31
Marketing Start
2019-08-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
46708519
Hyphenated Format
46708-519
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
ANDA212639 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (46708-519-10) / 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": "64e77f0a-fff5-4e24-9af2-38a14b9a4ef9", "openfda": {"unii": ["QZO5366EW7"], "rxcui": ["310015"], "spl_set_id": ["fb2e0729-b0bc-4c3f-9961-8bb38f84a032"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46708-519-10) / 10 mL in 1 BOTTLE", "package_ndc": "46708-519-10", "marketing_start_date": "20190809"}], "brand_name": "Dorzolamide Hydrochloride", "product_id": "46708-519_64e77f0a-fff5-4e24-9af2-38a14b9a4ef9", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]"], "product_ndc": "46708-519", "generic_name": "Dorzolamide Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dorzolamide Hydrochloride", "active_ingredients": [{"name": "DORZOLAMIDE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA212639", "marketing_category": "ANDA", "marketing_start_date": "20190809", "listing_expiration_date": "20261231"}