What is NDC 43598-286?

43598-286 is the product NDC for Omeprazole, Omeprazole 20 mg/1 tablet, delayed release, listed with the FDA by Dr. Reddys Laboratories Inc. It has 7 package NDCs, shown above in 10- and 11-digit form.

Dr. Reddys Laboratories Inc, NDC labeler code 43598. 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 43598-286 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43598-286Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43598-0286Add 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
43598-286-25	4359802862543598028625	2 BLISTER PACK in 1 CARTON (43598-286-25) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKMarketed from Nov 6, 2018
43598-286-27	4359802862743598028627	2 BOTTLE in 1 CARTON (43598-286-27) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)Marketed from Nov 6, 2018
43598-286-32	4359802863243598028632	2 BLISTER PACK in 1 CARTON (43598-286-32) / 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK (43598-286-70)Marketed from Nov 6, 2018
43598-286-33	4359802863343598028633	3 BOTTLE in 1 CARTON (43598-286-33) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)Marketed from Nov 6, 2018
43598-286-37	4359802863743598028637	3 BLISTER PACK in 1 CARTON (43598-286-37) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKMarketed from Nov 6, 2018
43598-286-52	4359802865243598028652	14 TABLET, DELAYED RELEASE in 1 BOTTLE (43598-286-52)Marketed from Nov 6, 2018
43598-286-74	4359802867443598028674	1 BLISTER PACK in 1 CARTON (43598-286-74) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKMarketed from Nov 6, 2018

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: Tablet, Delayed release
Route: Oral
Labeler: Dr. Reddys Laboratories IncNDC labeler code 43598
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207740
Marketing start: Nov 6, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers: Product ID 43598-286_ccd2bf38-c7b2-b12e-14a6-ca3631d9dfd4SPL ID ccd2bf38-c7b2-b12e-14a6-ca3631d9dfd4SPL set ID 4b3b389d-a151-d851-cb05-64eb49979e5eRxCUI 402014UNII KG60484QX9
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

N443598028625 followed by a unit qualifier and the quantity

Package 43598-0286-25. 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 Dec 19, 2024.

Indications (excerpt from the label)

Use(s) treats frequent heartburn (occurs 2 or more days a week) not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43598-286

What is NDC 43598-286?: 43598-286 is the product NDC for Omeprazole, Omeprazole 20 mg/1 tablet, delayed release, listed with the FDA by Dr. Reddys Laboratories Inc. It has 7 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. Reddys Laboratories Inc, NDC labeler code 43598. 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 207740

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

FDA NDC Directory listings under ANDA 207740
Product	Strength	Form · route	Labeler	Product NDC
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	Walgreens Company	0363-1607
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	Dr. Reddys Laboratories Inc	43598-841
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	AMERISOURCEBERGEN DRUG CORPORATION	46122-739
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	BluePoint Laboratories	68001-441
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	Walmart Inc.	79903-305
Omeprazole	Omeprazole 20 mg/1	Tablet, Delayed releaseOral	Chain Drug Marketing Association INC	83324-141