Web 2.0 Resource for the FDA
LATISSE
Drug Names(s)
LATISSE
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FDA Application No
(NDA) 022369
Active Ingredient(s)
BIMATOPROST
Company
ALLERGAN
Chemical Type
6 New indication
Review Classification
P Priority review drug
Products on Application (NDA) 022369
Drugname
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
LATISSE
BIMATOPROST
0.03%
SOLUTION/DROPS; TOPICAL
Prescription
Yes
Approval History
Action Date
Supplement Number
Action
Documents
Note
2008-12-24
000
Approval
Letter
Label
Review
Summary Review
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