Pantoprazole Sodium

Product NDC
71610-341
11-digit product format
716100341
Labeler code
71610
Product ID
71610-341_cde1734e-621c-470f-9254-abec4eb18c0e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pantoprazole Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA077056
Marketing category
ANDA
Marketing start
2007-12-21
Marketing end
2020-05-31
Substance
PANTOPRAZOLE SODIUM
Active strength
20 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71610-341-09EA - Each71610-341e910a594-d090-4d4b-b761-f612900de74412019-10-07
71610-341-29EA - Each71610-341572002bb-be64-4c04-b94c-03b1c6876a6812019-10-07