NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6888Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6888Add 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
50090-6888-0500906888002 BOTTLE in 1 CARTON (50090-6888-0) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMarketed from Dec 6, 2023

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
Omeprazole20 mg/1
Dosage form
Tablet, Delayed release
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211732
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 50090-6888_bf0ee06f-ffce-4ac6-9680-2425f8f7a887SPL ID bf0ee06f-ffce-4ac6-9680-2425f8f7a887SPL set ID a52842ac-ac9d-4344-9823-b8b2afb07903RxCUI 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

N450090688800 followed by a unit qualifier and the quantity

Package 50090-6888-00. 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)

Use • 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)

Other NDCs under ANDA 211732

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

FDA NDC Directory listings under ANDA 211732
ProductStrengthForm · routeLabelerProduct NDC
GoodMeds 24HR Acid Reducer Omeprazole 20mgomeprazole 20mgOmeprazole 20 mg/1Tablet, Delayed releaseOralCabinet Health P.B.C.82725-4052
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralCHAIN DRUG MARKETING ASSOCIATION, INC.83324-011
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralAllegiant Health69168-476
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralCamber Consumer Care Inc69230-318

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