Pantoprazole Sodium

Product NDC
55700-318
11-digit product format
557000318
Labeler code
55700
Product ID
55700-318_6f9a6a4b-284f-4acc-81d5-d6cd9bcd9472
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
pantoprazole sodium
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA090970
Marketing category
ANDA
Marketing start
2011-01-19
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-318-30EA - Each55700-3180888a6c0-cd72-4d88-bce7-006ced971b7412016-02-04
55700-318-60EA - Each55700-318d62ba920-0bf4-4d5c-ab20-09909b0c849112016-02-04
55700-318-90EA - Each55700-318e61ee99a-09d0-4798-9e12-e0f9f5512d5412017-09-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
55700-318-305570003183030 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-318-30) 2011-01-190000-00-00NoNoCurrent
55700-318-605570003186060 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-318-60) 2011-01-190000-00-00NoNoCurrent