Rabeprazole Sodium

Product NDC
68788-7143
11-digit product format
687887143
Labeler code
68788
Product ID
68788-7143_5627c9c5-3a49-4ff1-8515-461231402e8e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
RABEPRAZOLE SODIUM
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA204237
Marketing category
ANDA
Marketing start
2018-04-20
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7143-3EA - Each68788-714345bf366f-af18-4f33-8207-8e4c95141e6f12018-06-11
68788-7143-6EA - Each68788-7143dc3846a4-5b29-447a-92b1-94feedd9b72612018-06-11