Esomeprazole magnesium

Product NDC
68788-7442
11-digit product format
687887442
Labeler code
68788
Product ID
68788-7442_a6429847-a3a9-4a47-a974-3a26334d96be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Esomeprazole magnesium
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA208333
Marketing category
ANDA
Marketing start
2017-10-20
Marketing end
0000-00-00
Substance
ESOMEPRAZOLE MAGNESIUM
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
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7442-1EA - Each68788-744227598d65-c654-423b-b980-b16881143a7512020-04-20
68788-7442-2EA - Each68788-7442383962c7-48a0-4cda-b74e-0da24c58baf212020-04-20
68788-7442-3EA - Each68788-74424331d855-b423-4eee-b917-0309bef7bde612020-04-20
68788-7442-6EA - Each68788-744291b72f2a-8838-4168-b5d0-f4f86d7c59d012020-04-20
68788-7442-9EA - Each68788-7442711be0bc-aa75-4429-8747-250c01db419112020-04-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7442-168788744201100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7442-1) 2019-10-310000-00-00NoNoCurrent
68788-7442-26878874420220 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7442-2) 2019-10-310000-00-00NoNoCurrent
68788-7442-36878874420330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7442-3) 2019-10-310000-00-00NoNoCurrent
68788-7442-66878874420660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7442-6) 2019-10-310000-00-00NoNoCurrent
68788-7442-96878874420990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7442-9) 2019-10-310000-00-00NoNoCurrent