Prevacid

Product NDC
0067-6286
11-digit product format
000676286
Labeler code
0067
Product ID
0067-6286_7f6cc3d5-6355-48cb-b50a-958b1e96aa90
Type
HUMAN OTC DRUG
Nonproprietary name
Lansoprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Application
NDA022327
Marketing category
NDA
Marketing start
2009-10-12
Marketing end
2022-08-31
Substance
LANSOPRAZOLE
Active strength
15 mg/1
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
0067-6286-14EA - Each0067-628605f22d41-73b0-4c5e-877b-02b6f3be53bd12012-07-24
0067-6286-28EA - Each0067-628620086176-4cda-4d36-9049-fa0f1104a86412012-07-24
0067-6286-42EA - Each0067-628643b7f158-53a6-437e-9697-562cd0256a7d12012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0067-6286-14000676286141 BOTTLE in 1 CARTON (0067-6286-14) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE1 bottle2009-10-122022-08-31NoNoCurrent
0067-6286-28000676286282 BOTTLE in 1 PACKAGE, COMBINATION (0067-6286-28) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE2 bottle2009-10-122022-08-31NoNoCurrent
0067-6286-42000676286423 BOTTLE in 1 PACKAGE, COMBINATION (0067-6286-42) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE3 bottle2009-10-122022-08-31NoNoCurrent