Prevacid

Product NDC
70518-0502
11-digit product format
705180502
Labeler code
70518
Product ID
70518-0502_8583b866-fe1e-8be1-e053-2991aa0ae5d6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lansoprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
NDA020406
Marketing category
NDA
Marketing start
2017-05-09
Marketing end
0000-00-00
Substance
LANSOPRAZOLE
Active strength
30 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record