What is NDC 55111-157?

55111-157 is the product NDC for Omeprazole, Omeprazole 10 mg/1 capsule, delayed release, listed with the FDA by Dr. Reddy's Laboratories Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.

Dr. Reddy's Laboratories Limited, NDC labeler code 55111. 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 55111-157 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)55111-157Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55111-0157Add 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
55111-157-01	5511101570155111015701	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-157-01)Marketed from Jan 21, 2009
55111-157-10	5511101571055111015710	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-157-10)Marketed from Jan 21, 2009
55111-157-30	5511101573055111015730	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-157-30)Marketed from Jan 21, 2009
55111-157-78	5511101577855111015778	10 BLISTER PACK in 1 CARTON (55111-157-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-157-79)Marketed from Jan 21, 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 — 10 mg/1
Dosage form: Capsule, Delayed release
Route: Oral
Labeler: Dr. Reddy's Laboratories LimitedNDC labeler code 55111
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075576
Marketing start: Jan 21, 2009
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 55111-157_0dc50704-e0d5-1fcc-b0b5-6e5556db65e8SPL ID 0dc50704-e0d5-1fcc-b0b5-6e5556db65e8SPL set ID 72fb11b6-b08c-2f02-d82b-f60f52394903RxCUI 198051, 199119, 200329UNII KG60484QX9UPC 0355111157304
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

N455111015701 followed by a unit qualifier and the quantity

Package 55111-0157-01. 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 15, 2024.

Indications (excerpt from the label)

Omeprazole 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 2 years of age and older (1.4) • Maintenance of healing of EE due to acid-mediated GERD in patients 2 years of age and older (1.6) • Pathologic hypersecretory conditions in adults (1.7) 1.1 Treatment of Active Duodenal Ulcer Omeprazole delayed-release capsules are indicated for short-term treatment of active duodenal ulcer in adults. Most patie…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55111-157

What is NDC 55111-157?: 55111-157 is the product NDC for Omeprazole, Omeprazole 10 mg/1 capsule, delayed release, listed with the FDA by Dr. Reddy's Laboratories Limited. 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?: Dr. Reddy's Laboratories Limited, NDC labeler code 55111. 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 magnesium 20 mg/1	Capsule, Delayed releaseOral	Chain Drug Marketing Association, Inc.	83324-309	83324-0309-1483324-0309-42
Omeprazole	Omeprazole 20 mg/1	Tablet, Orally disintegrating, Delayed releaseOral	Amazon.com Services LLC	72288-666	72288-0666-5572288-0666-74
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	Discount Drug Mart, Inc	53943-038	53943-0038-1453943-0038-42
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

All 253 Omeprazole NDCs

Other NDCs under ANDA 075576

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

FDA NDC Directory listings under ANDA 075576
Product	Strength	Form · route	Labeler	Product NDC
Omeprazole	Omeprazole 10 mg/1	Capsule, Delayed releaseOral	Proficient Rx LP	63187-805
Omeprazole	Omeprazole 10 mg/1	Capsule, Delayed releaseOral	QPharma, Inc.	42708-158
Omeprazole	Omeprazole 10 mg/1	Capsule, Delayed releaseOral	NorthStar Rx LLC	16714-714
Omeprazole DRomeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0071
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Advanced Rx of Tennessee, LLC	80425-0415
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Quality Care Products, LLC	49999-265
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Quallent Pharmaceuticals Health LLC	82009-022
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Northwind Health Company, LLC	51655-061
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Bryant Ranch Prepack	71335-0332
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Dr. Reddy's Laboratories Limited	55111-158
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Dr. Reddy's Laboratories Limited	55111-159
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-1157
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	St. Mary's Medical Park Pharmacy	60760-833
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	PD-Rx Pharmaceuticals, Inc.	43063-743