NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0332Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0332Add 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
71335-0332-071335033200713350332007 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-0)Marketed from May 28, 2024
71335-0332-1713350332017133503320130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-1)Marketed from Jul 16, 2018
71335-0332-2713350332027133503320260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-2)Marketed from Mar 25, 2020
71335-0332-3713350332037133503320356 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-3)Marketed from May 28, 2024
71335-0332-4713350332047133503320490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-4)Marketed from May 8, 2020
71335-0332-5713350332057133503320520 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-5)Marketed from Jun 3, 2020
71335-0332-6713350332067133503320615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-6)Marketed from Jul 6, 2018
71335-0332-77133503320771335033207120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-7)Marketed from Mar 12, 2020
71335-0332-87133503320871335033208100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-8)Marketed from May 28, 2024
71335-0332-9713350332097133503320928 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-9)Marketed from May 28, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075576
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 71335-0332_a400ebb3-e9ae-4db8-90b1-da9a9527230eSPL ID a400ebb3-e9ae-4db8-90b1-da9a9527230eSPL set ID e1f20429-cfaa-420b-a65a-271be37eb799RxCUI 198051UNII 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

N471335033200 followed by a unit qualifier and the quantity

Package 71335-0332-00. 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 .

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 71335-0332

What is NDC 71335-0332?
71335-0332 is the product NDC for Omeprazole, Omeprazole 20 mg/1 capsule, delayed release, listed with the FDA by Bryant Ranch Prepack. It has 10 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?
Bryant Ranch Prepack, NDC labeler code 71335. 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 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
ProductStrengthForm · routeLabelerProduct NDC
OmeprazoleOmeprazole 10 mg/1Capsule, Delayed releaseOralProficient Rx LP63187-805
OmeprazoleOmeprazole 10 mg/1Capsule, Delayed releaseOralQPharma, Inc.42708-158
OmeprazoleOmeprazole 10 mg/1Capsule, Delayed releaseOralNorthStar Rx LLC16714-714
Omeprazole DRomeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralAdvanced Rx of Tennessee, LLC80425-0071
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralAdvanced Rx of Tennessee, LLC80425-0415
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralQuality Care Products, LLC49999-265
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralQuallent Pharmaceuticals Health LLC82009-022
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralNorthwind Health Company, LLC51655-061
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralDr. Reddy's Laboratories Limited55111-158
OmeprazoleOmeprazole 10 mg/1Capsule, Delayed releaseOralDr. Reddy's Laboratories Limited55111-157
OmeprazoleOmeprazole 40 mg/1Capsule, Delayed releaseOralDr. Reddy's Laboratories Limited55111-159
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralA-S Medication Solutions50090-1157
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralSt. Mary's Medical Park Pharmacy60760-833
OmeprazoleOmeprazole 20 mg/1Capsule, Delayed releaseOralPD-Rx Pharmaceuticals, Inc.43063-743

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