Pantoprazole Sodium

Product NDC
50090-2295
11-digit product format
500902295
Labeler code
50090
Product ID
50090-2295_fe8d1dd5-e59d-4d94-ab4c-73a1e7d34cf2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pantoprazole Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078281
Marketing category
ANDA
Marketing start
2011-01-20
Marketing end
0000-00-00
Substance
PANTOPRAZOLE SODIUM
Active strength
40 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2295-0EA - Each50090-2295017717f9-3291-4d30-9a44-4d836cd08ae812019-02-13
50090-2295-1EA - Each50090-2295c1ab4e5c-b14a-406f-a1d6-a9700deaba2e12018-12-13