Omeprazole

Product NDC
50090-3060
11-digit product format
500903060
Labeler code
50090
Product ID
50090-3060_688020a9-2d66-4e06-8f33-4cccf21b7614
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Omeprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203270
Marketing category
ANDA
Marketing start
2015-08-19
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
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3060-0EA - Each50090-3060b1b19aa3-1619-4360-ac67-7fe7dc5f619312019-05-02
50090-3060-2EA - Each50090-3060956af949-a4cf-403c-aa2e-38836ce8f6be12020-02-13
50090-3060-3EA - Each50090-306065cfbc42-0636-417f-9b7e-b661d623454a12020-02-13
50090-3060-5EA - Each50090-30601bad6b4a-3387-4db3-8034-4d623ded05e112020-02-13
50090-3060-6EA - Each50090-306038c45445-864e-4baa-9b3f-99ca984c47e212020-02-13
50090-3060-7EA - Each50090-3060dfd2e9c5-58bc-46f0-a3f4-c877772a9ffc12020-02-13
50090-3060-8EA - Each50090-30604139fd52-33e0-42f5-bb7e-9e26f391879e12020-02-13
50090-3060-9EA - Each50090-3060862c13ef-fc62-4565-af16-964d8337f2a012020-02-13