Tim-Dor-Lat
Approved
Approval ID
6bb40362-ff91-4c3e-e053-2a91aa0ab66a
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 - Latanoprost PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70261-521
Product Classification
G
Generic Name
Timolol - Dorzolamide - Latanoprost PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateMay 8, 2018
FDA Product Classification
INGREDIENTS (3)
DORZOLAMIDE HYDROCHLORIDEActive
Quantity: 20 mg in 1 mL
Code: QZO5366EW7
Classification: ACTIM
LATANOPROSTActive
Quantity: 0.05 mg in 1 mL
Code: 6Z5B6HVF6O
Classification: ACTIB
TIMOLOL MALEATEActive
Quantity: 5 mg in 1 mL
Code: P8Y54F701R
Classification: ACTIM