Tim-Dor PF
Approved
Approval ID
6bb5919c-dd14-10e8-e053-2991aa0a6695
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.
Timolol - Dorzolamide PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70261-519
Product Classification
G
Generic Name
Timolol - Dorzolamide PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateMay 8, 2018
FDA Product Classification
INGREDIENTS (2)
TIMOLOL MALEATEActive
Quantity: 5 mg in 1 mL
Code: P8Y54F701R
Classification: ACTIM
DORZOLAMIDE HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: QZO5366EW7
Classification: ACTIM