Tim-Lat -PF
Approved
Approval ID
6bb5e498-b27c-191a-e053-2a91aa0acab3
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-Latanoprost PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code70261-517
Product Classification
G
Generic Name
Timolol-Latanoprost PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateMay 8, 2018
FDA Product Classification
INGREDIENTS (3)
TIMOLOL MALEATEActive
Quantity: 5 mg in 1 mL
Code: P8Y54F701R
Classification: ACTIM
LATANOPROSTActive
Quantity: 0.05 mg in 1 mL
Code: 6Z5B6HVF6O
Classification: ACTIB
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUSInactive
Quantity: 1 mg in 1 mL
Code: KH7I04HPUU
Classification: IACT