Omeprazole

Product NDC
60760-396
11-digit product format
607600396
Labeler code
60760
Product ID
60760-396_7b32c52a-f26c-4acc-e053-2a91aa0a5bcc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Omeprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA091672
Marketing category
ANDA
Marketing start
2018-03-05
Marketing end
0000-00-00
Substance
OMEPRAZOLE
Active strength
20 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
60760-396-05607600396055 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-396-05) 2018-10-300000-00-00NoNoCurrent
60760-396-07607600396077 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-396-07) 2018-03-050000-00-00NoNoCurrent
60760-396-206076003962020 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-396-20) 2018-06-060000-00-00NoNoCurrent
60760-396-306076003963030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-396-30) 2018-03-050000-00-00NoNoCurrent
60760-396-606076003966060 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-396-60) 2018-03-130000-00-00NoNoCurrent
60760-396-906076003969090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-396-90) 2018-03-280000-00-00NoNoCurrent