NDC 41163-614

equaline omeprazole delayed release

Omeprazole

equaline omeprazole delayed release is a Oral Tablet, Delayed Release in the Human Otc Drug category. It is labeled and distributed by Supervalu Inc. The primary component is Omeprazole.

Product ID41163-614_0fb03f07-3c26-49fa-b192-436c66ad22b6
NDC41163-614
Product TypeHuman Otc Drug
Proprietary Nameequaline omeprazole delayed release
Generic NameOmeprazole
Dosage FormTablet, Delayed Release
Route of AdministrationORAL
Marketing Start Date2021-08-20
Marketing CategoryNDA /
Application NumberNDA022032
Labeler NameSupervalu Inc
Substance NameOMEPRAZOLE
Active Ingredient Strength20 mg/1
Pharm ClassesCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 41163-614-01

1 BOTTLE in 1 CARTON (41163-614-01) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE
Marketing Start Date2021-08-20
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "equaline omeprazole delayed release" or generic name "Omeprazole"

NDCBrand NameGeneric Name
0363-1008Acid ReducerOmeprazole
0536-1322Acid ReducerOmeprazole
0113-7401Basic Care OmeprazoleOmeprazole
0113-7520basic care omeprazoleomeprazole
0113-7915Basic Care OmeprazoleOmeprazole
0113-0520good sense omeprazoleomeprazole
0113-0915Good Sense OmeprazoleOmeprazole
0113-1723Good Sense OmeprazoleOmeprazole
0113-1803good sense omeprazole delayed releaseomeprazole
0093-5294OmeprazoleOmeprazole
0363-0007omeprazoleOmeprazole
0363-0915omeprazoleOmeprazole
0363-1607OmeprazoleOmeprazole
0363-1819omeprazoleomeprazole
0378-5211Omeprazoleomeprazole
0378-5222Omeprazoleomeprazole
0378-6150Omeprazoleomeprazole
0615-1359OmeprazoleOmeprazole
0615-2302OmeprazoleOmeprazole
0615-2305OmeprazoleOmeprazole
0615-7933OmeprazoleOmeprazole
0615-8079OmeprazoleOmeprazole
0615-8320OmeprazoleOmeprazole
0615-8406OmeprazoleOmeprazole
0781-2234OmeprazoleOmeprazole
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