What is NDC 62175-114?

62175-114 is the product NDC for Omeprazole, Omeprazole 10 mg/1 capsule, delayed release, listed with the FDA by Lannett Company, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Omeprazole NDC 62175-114 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62175-114Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62175-0114Add 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 NDC	11-digit (billing)	Package
62175-114-32	62175011432	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-32)Marketed from Sep 3, 2003
62175-114-37	62175011437	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-37)Marketed from Sep 3, 2003
62175-114-46	62175011446	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-46)Marketed from Sep 3, 2003
62175-114-49	62175011449	72000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-114-49)Marketed from Sep 3, 2003

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 — 10 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: Sep 3, 2003
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 62175-114_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

N462175011432 followed by a unit qualifier and the quantity

Package 62175-0114-32. 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

Current FDA label (SPL), effective Apr 21, 2023.

Indications (excerpt from the label)

Omeprazole Delayed-Release Capsules is a proton pump inhibitor (PPI) indicated for the: Treatment of active duodenal ulcer in adults (1.1) Eradication of Helicobacter pylori to reduce the risk of duodenal ulcer recurrence in adults (1.2) Treatment of active benign gastric ulcer in adults (1.3) Treatment of symptomatic gastroesophageal reflux disease (GERD) in patients 1 year of age and older (1.4) Treatment of erosive esophagitis (EE) due to acid-mediated GERD in patients 1 year of age and older (1.5) Maintenance of healing of EE due to acid-mediated GERD in patients 1 year of age and older (1.6) Pathologic hypersecretory conditions in adults (1.7) 1.1 Treatment of Active Duodenal Ulcer Omep…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62175-114

What is NDC 62175-114?: 62175-114 is the product NDC for Omeprazole, Omeprazole 10 mg/1 capsule, delayed release, listed with the FDA by Lannett Company, Inc.. It has 4 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Omeprazole	Omeprazole 20 mg/1	Tablet, Orally disintegrating, Delayed releaseOral	Amazon.com Services LLC	72288-666	72288-0666-55
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	Discount Drug Mart, Inc	53943-038	53943-0038-1453943-0038-42
Omeprazoleomeprazole magnesium	Omeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	YYBA CORP	73581-015	73581-0015-03
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	Amazon.com Services LLC	72288-934	72288-0934-01
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	H E B	59640-699	59640-0699-0159640-0699-03
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Unit Dose Solutions, Inc.	87441-063	87441-0063-01
Omeprazole	Omeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	Safeway	21130-783	21130-0783-0121130-0783-03
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Preferred Phharmaceuticals Inc.	68788-4104	68788-4104-0168788-4104-0268788-4104-03+4 more
omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Amazon.com Services LLC	72288-606	72288-0606-03
Omeprazole	Omeprazole magnesium 20 mg/1	Capsule, Delayed releaseOral	Walgreen Company	0363-4099	00363-4099-03

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
Product	Strength	Form · route	Labeler	Product NDC
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Lannett Company, Inc.	62175-118
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Lannett Company, Inc.	62175-136
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Bryant Ranch Prepack	71335-1746
Omeprazole	Omeprazole 10 mg/1	Capsule, Delayed releaseOral	Chartwell RX, LLC	62135-530
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-2243
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Aphena Pharma Solutions - Tennessee, LLC	43353-829
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Bryant Ranch Prepack	71335-1532
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Proficient Rx LP	71205-157
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-4906
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	NuCare Pharmaceuticals,Inc.	68071-4025
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	PD-Rx Pharmaceuticals, Inc.	72789-155