esomeprazole magnesium

Product NDC
68788-7615
11-digit product format
687887615
Labeler code
68788
Product ID
68788-7615_950b778e-131f-463b-809e-d807f5b62c1b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
esomeprazole magnesium
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA206296
Marketing category
ANDA
Marketing start
2020-02-07
Marketing end
0000-00-00
Substance
ESOMEPRAZOLE MAGNESIUM DIHYDRATE
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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7615-1EA - Each68788-7615e68908a0-f170-4cd8-935e-5dcc356750aa12020-03-10
68788-7615-2EA - Each68788-761572852ad2-c87b-4f8d-815b-50804f6d970112020-03-10
68788-7615-3EA - Each68788-7615abe86c8f-25db-4975-a336-61805f8d68ca12020-03-10
68788-7615-6EA - Each68788-7615abf9fb12-7874-4679-a273-58f3aac7863312020-03-10
68788-7615-9EA - Each68788-7615d04f80f0-0d56-48bb-9612-d56a08538dff12020-03-10

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68788-7615-168788761501100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7615-1) 2020-02-070000-00-00NoNoCurrent
68788-7615-26878876150220 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7615-2) 2020-02-070000-00-00NoNoCurrent
68788-7615-36878876150330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7615-3) 2020-02-070000-00-00NoNoCurrent
68788-7615-66878876150660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7615-6) 2020-02-070000-00-00NoNoCurrent
68788-7615-96878876150990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7615-9) 2020-02-070000-00-00NoNoCurrent