Omeprazole

Product NDC

0615-2302

11-digit product format

006152302

Labeler code

0615

Product ID

0615-2302_e3144ea7-4181-4efd-b95b-6fe3c6440cbf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Omeprazole

Dosage form

CAPSULE, DELAYED RELEASE

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA075576

Marketing category

ANDA

Marketing start

2007-10-22

Marketing end

0000-00-00

Substance

OMEPRAZOLE

Active strength

40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record