Pantoprazole Sodium

Product NDC
0615-8308
11-digit product format
006158308
Labeler code
0615
Product ID
0615-8308_73b8ba6a-f654-468d-b19d-a68a833576fc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pantoprazole Sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Application
ANDA078281
Marketing category
ANDA
Marketing start
2011-01-20
Marketing end
2023-07-31
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
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0615-8308-050061583080515 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8308-05) 2019-07-032023-07-31NoNoCurrent
0615-8308-07006158308077 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8308-07) 2019-07-032023-07-31NoNoCurrent
0615-8308-140061583081414 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8308-14) 2019-07-032023-07-31NoNoCurrent
0615-8308-30006158308306 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8308-30) > 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK6 blister pack2019-07-022023-07-31NoNoCurrent
0615-8308-390061583083930 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8308-39) 2019-07-032023-07-31NoNoCurrent