TIMOLOL MALEATE
1163 TIMOLOL MALEATE
Approved
Approval ID
92c79a2d-f3b6-236b-e053-2a95a90a06a7
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 17, 2019
Manufacturers
FDA
H.J. Harkins Company, Inc.
DUNS: 147681894
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
TIMOLOL MALEATE
PRODUCT DETAILS
NDC Product Code76519-1163
Application NumberANDA077259
Marketing CategoryC73584
Route of AdministrationOPHTHALMIC
Effective DateSeptember 17, 2019
Generic NameTIMOLOL MALEATE
INGREDIENTS (1)
TIMOLOL MALEATEActive
Quantity: 0.1 mg in 1 mL
Code: P8Y54F701R
Classification: ACTIM