What is NDC 70700-150?

70700-150 is the product NDC for Omeprazole, Omeprazole 20 mg/1 capsule, delayed release, listed with the FDA by Xiromed, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

Xiromed, LLC, NDC labeler code 70700. 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 70700-150 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70700-150Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70700-0150Add 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
70700-150-00	7070001500070700015000	1 CAPSULE, DELAYED RELEASE in 1 PAIL (70700-150-00)Marketed from Mar 17, 2022
70700-150-01	7070001500170700015001	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-150-01)Marketed from Jan 8, 2021
70700-150-10	7070001501070700015010	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-150-10)Marketed from Feb 20, 2019
70700-150-30	7070001503070700015030	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70700-150-30)Marketed from Feb 20, 2019

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 — 20 mg/1
Dosage form: Capsule, Delayed release
Route: Oral
Labeler: Xiromed, LLCNDC labeler code 70700
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212977
Marketing start: Feb 20, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 70700-150_49528611-b139-6768-e43e-bc6f26715fa3SPL ID 49528611-b139-6768-e43e-bc6f26715fa3SPL set ID 38bd8e13-591e-f11b-7d8a-11717c56493cRxCUI 198051, 199119, 200329UNII KG60484QX9UPC 0370700150016, 0370700149300
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

N470700015000 followed by a unit qualifier and the quantity

Package 70700-0150-00. 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 Feb 15, 2022.

Indications (excerpt from the label)

Omeprazole delayed-release capsules are 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 ) • Treatment of erosive esophagitis (EE) due to acid-mediated GERD in patients 2 years of age and older ( 1.5 ) • 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 Treatme…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70700-150

What is NDC 70700-150?: 70700-150 is the product NDC for Omeprazole, Omeprazole 20 mg/1 capsule, delayed release, listed with the FDA by Xiromed, LLC. 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?: Xiromed, LLC, NDC labeler code 70700. 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 212977

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

FDA NDC Directory listings under ANDA 212977
Product	Strength	Form · route	Labeler	Product NDC
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-813
Omeprazole	Omeprazole 10 mg/1	Capsule, Delayed releaseOral	Xiromed, LLC	70700-149
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Xiromed, LLC	70700-151
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-880
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-663
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-5901
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	A-S Medication Solutions	50090-5902
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8406
Omeprazole	Omeprazole 40 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-943
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Aphena Pharma Solutions - Tennessee, LLC	71610-963
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Boswell Pharmacy Services LLC d/b/a BPS Wholesale	83209-150
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-641
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Proficient Rx LP	71205-613
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	REMEDYREPACK INC.	70518-3278
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Proficient Rx LP	71205-907
Omeprazole	Omeprazole 20 mg/1	Capsule, Delayed releaseOral	Golden State Medical Supply, Inc.	51407-287