RABEPRAZOLE SODIUM

Product NDC
68788-6864
11-digit product format
687886864
Labeler code
68788
Product ID
68788-6864_9efd84cc-37f1-43b2-a061-4c9eba966c50
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
RABEPRAZOLE SODIUM
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA078964
Marketing category
ANDA
Marketing start
2017-01-04
Marketing end
0000-00-00
Substance
RABEPRAZOLE SODIUM
Active strength
20 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record