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FDA Approval

Tim-Brim-Dor PF

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
ImprimisRx NJ
DUNS: 931390178
Effective Date
May 8, 2018
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Timolol(5 mg in 1 mL)
Dorzolamide(20 mg in 1 mL)
Brimonidine(1.5 mg in 1 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Tim-Brim-Dor PF

Product Details

NDC Product Code
70261-520
Route of Administration
OPHTHALMIC
Effective Date
May 8, 2018
TimololActive
Code: P8Y54F701RClass: ACTIMQuantity: 5 mg in 1 mL
Code: QZO5366EW7Class: ACTIMQuantity: 20 mg in 1 mL
Code: 4S9CL2DY2HClass: ACTIMQuantity: 1.5 mg in 1 mL
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