NDC codes

FDA NDC Directory
Product NDC (as listed)62175-136Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62175-0136Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
62175-136-32621750136326217501363230 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-32)Marketed from Jan 23, 2009
62175-136-376217501363762175013637100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-37)Marketed from Jan 23, 2009
62175-136-4362175013643621750136431000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-43)Marketed from Jan 23, 2009
62175-136-46621750136466217501364690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-46)Marketed from Jan 23, 2009
62175-136-49621750136496217501364936000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-136-49)Marketed from Jan 23, 2009

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Omeprazole
Generic name (nonproprietary)
omeprazole
Active ingredients
Omeprazole — 40 mg/1
Dosage form
Capsule, Delayed release
Route
Oral
Labeler
Lannett Company, Inc.NDC labeler code 62175
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075410
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 62175-136_e786b865-dc62-4018-9cb1-7056b7ca2cdeSPL ID e786b865-dc62-4018-9cb1-7056b7ca2cdeSPL set ID 92201fb1-4570-42db-8da3-3b8c0e291d32RxCUI 198051, 199119, 200329UNII KG60484QX9UPC 0362175136329, 0362175114327, 0362175118325
Pharmacologic class
Proton Pump Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462175013632 followed by a unit qualifier and the quantity

Package 62175-0136-32. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 62175-136

What is NDC 62175-136?
62175-136 is the product NDC for Omeprazole, Omeprazole 40 mg/1 capsule, delayed release, listed with the FDA by Lannett Company, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Omeprazole.
What is the active ingredient?
Omeprazole.
Who is the labeler?
Lannett Company, Inc., NDC labeler code 62175. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Omeprazole?
252 other product NDCs are listed under this name. See all Omeprazole NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Omeprazole NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
OmeprazoleOmeprazole magnesium 20 mg/1Capsule, Delayed releaseOralChain Drug Marketing Association, Inc.83324-30983324-0309-1483324-0309-42
OmeprazoleOmeprazole 20 mg/1Tablet, Orally disintegrating, Delayed releaseOralAmazon.com Services LLC72288-66672288-0666-5572288-0666-74
Omeprazoleomeprazole magnesiumOmeprazole magnesium 20 mg/1Capsule, Delayed releaseOralYYBA CORP73581-01573581-0015-03
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralDiscount Drug Mart, Inc53943-03853943-0038-1453943-0038-42
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralAmazon.com Services LLC72288-93472288-0934-01
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralH E B59640-69959640-0699-0159640-0699-03
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralUnit Dose Solutions, Inc.87441-06387441-0063-01
OmeprazoleOmeprazole magnesium 20 mg/1Capsule, Delayed releaseOralSafeway21130-78321130-0783-0121130-0783-03
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralPreferred Phharmaceuticals Inc.68788-410468788-4104-0168788-4104-0268788-4104-03+4 more
omeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralAmazon.com Services LLC72288-60672288-0606-03

All 253 Omeprazole NDCs

Other NDCs under ANDA 075410

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 075410
ProductStrengthForm · routeLabelerProduct NDC
OmeprazoleOmeprazole 40 mg/1Capsule, Delayed releaseOralNuCare Pharmaceuticals,Inc.68071-4906
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralNuCare Pharmaceuticals,Inc.68071-4025
OmeprazoleOmeprazole 40 mg/1Capsule, Delayed releaseOralProficient Rx LP71205-157
OmeprazoleOmeprazole 40 mg/1Capsule, Delayed releaseOralBryant Ranch Prepack71335-1532
OmeprazoleOmeprazole 10 mg/1Capsule, Delayed releaseOralLannett Company, Inc.62175-114
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralLannett Company, Inc.62175-118
OmeprazoleOmeprazole 40 mg/1Capsule, Delayed releaseOralPD-Rx Pharmaceuticals, Inc.72789-155
OmeprazoleOmeprazole 40 mg/1Capsule, Delayed releaseOralAphena Pharma Solutions - Tennessee, LLC43353-829
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralBryant Ranch Prepack71335-1746
OmeprazoleOmeprazole 10 mg/1Capsule, Delayed releaseOralChartwell RX, LLC62135-530
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralNuCare Pharmaceuticals,Inc.68071-2243

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