Lansoprazole

Product NDC
0536-1236
11-digit product format
005361236
Labeler code
0536
Product ID
0536-1236_203d8bb1-2b31-4392-9eab-5bb15b9b3d02
Type
HUMAN OTC DRUG
Nonproprietary name
Lansoprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Rugby Laboratories, Inc.
Application
ANDA203187
Marketing category
ANDA
Marketing start
2019-05-31
Marketing end
0000-00-00
Substance
LANSOPRAZOLE
Active strength
15 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
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
0536-1236-13EA - Each0536-12364dedd9e3-8f8c-46b4-864c-ab4601f1808412020-01-03
0536-1236-88EA - Each0536-1236b3174a3a-eb26-4eb5-8a7e-6ef809d8314a12020-04-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0536-1236-13005361236133 BOTTLE, PLASTIC in 1 BOX (0536-1236-13) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC2019-05-310000-00-00NoNoCurrent
0536-1236-88005361236881 BOTTLE, PLASTIC in 1 BOX (0536-1236-88) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC2019-05-310000-00-00NoNoCurrent