Lansoprazole

Product NDC
55700-595
11-digit product format
557000595
Labeler code
55700
Product ID
55700-595_24329af4-94a2-4693-9832-28823a0533d8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lansoprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA091269
Marketing category
ANDA
Marketing start
2018-03-16
Marketing end
0000-00-00
Substance
LANSOPRAZOLE
Active strength
15 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
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
55700-595-60EA - Each55700-59534129d77-40cc-416c-9483-1d3bf2a176b212018-04-19