bimatoprost

Product NDC
57297-429
11-digit product format
572970429
Labeler code
57297
Product ID
57297-429_7e93fb29-97d9-4fa1-bdec-75eea81143c9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
bimatoprost
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Labeler
LUPIN LIMITED
Application
ANDA203991
Marketing category
ANDA
Marketing start
2015-05-13
Marketing end
0000-00-00
Substance
BIMATOPROST
Active strength
0 mg/mL
Pharmacologic classes
Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#