Dorzolamide PF
Approved
Approval ID
6bb681e9-0fc7-7e5c-e053-2991aa0a7c65
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 8, 2018
Manufacturers
FDA
ImprimisRx NJ
DUNS: 931390178
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Dorzolamide PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70261-516
Product Classification
G
Generic Name
Dorzolamide PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateMay 8, 2018
FDA Product Classification
INGREDIENTS (1)
DORZOLAMIDE HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: QZO5366EW7
Classification: ACTIM
Drug Labeling Information
STORAGE AND HANDLING SECTION
LOINC: 44425-7Updated: 1/1/2018
Store at 20° to 25° C (68° to 77° F)