NDC codes

FDA NDC Directory
Product NDC (as listed)82725-4052Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82725-4052Add 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
82725-4052-182725405201827254052013 BOTTLE in 1 CARTON (82725-4052-1) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMarketed from Aug 17, 2026

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

Generic name (nonproprietary)
omeprazole 20mg
Active ingredients
Omeprazole — 20 mg/1
Dosage form
Tablet, Delayed release
Route
Oral
Labeler
Cabinet Health P.B.C.NDC labeler code 82725
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 82725-4052_58c9c8ef-b92a-14eb-e063-6294a90a3761SPL ID 58c9c8ef-b92a-14eb-e063-6294a90a3761SPL set ID 58c9c8ef-b929-14eb-e063-6294a90a3761RxCUI 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

N482725405201 followed by a unit qualifier and the quantity

Package 82725-4052-01. 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 .

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)

About NDC 82725-4052

What is NDC 82725-4052?
82725-4052 is the product NDC for GoodMeds 24HR Acid Reducer Omeprazole 20mg, Omeprazole 20 mg/1 tablet, delayed release, listed with the FDA by Cabinet Health P.B.C.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
GoodMeds 24HR Acid Reducer Omeprazole 20mg (Omeprazole 20mg).
What is the active ingredient?
Omeprazole.
Who is the labeler?
Cabinet Health P.B.C., NDC labeler code 82725. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for GoodMeds 24HR Acid Reducer Omeprazole 20mg?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralA-S Medication Solutions50090-6888
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralAllegiant Health69168-476
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralCamber Consumer Care Inc69230-318
OmeprazoleOmeprazole 20 mg/1Tablet, Delayed releaseOralCHAIN DRUG MARKETING ASSOCIATION, INC.83324-011

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