NDC codes

FDA NDC Directory
Product NDC (as listed)30142-989Labeler and product segments. Claims need a package NDC.
Product NDC at billing width30142-0989Add 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
30142-989-28301420989282 BOTTLE in 1 CARTON (30142-989-28) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (30142-989-14)Marketed from Aug 7, 2020

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)
esomeprazole
Generic name (nonproprietary)
esomeprazole
Active ingredients
Esomeprazole magnesium — 20 mg/1
Dosage form
Capsule, Delayed release
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212866
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C19 Inhibitors (Mechanism)Proton Pump Inhibitors (Mechanism)
Identifiers
Product ID 30142-989_d1f98f06-8779-4753-af5f-b45fffea3d92SPL ID d1f98f06-8779-4753-af5f-b45fffea3d92SPL set ID 7fa75bbe-5b9f-49ca-84de-f80e5a858de4RxCUI 606726UNII R6DXU4WAY9UPC 0041260009938
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

N430142098928 followed by a unit qualifier and the quantity

Package 30142-0989-28. 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)

Uses 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 212866

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

FDA NDC Directory listings under ANDA 212866
ProductStrengthForm · routeLabelerProduct NDC
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralGERI-CARE PHARMACEUTICALS, CORP57896-740
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralOhm Laboratories Inc.51660-027
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralVALU MERCHANDISERS COMPANY63941-999
Esomeprazole MagnesiumEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralLITTLE PHARMA, INC.72559-011
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium 20 mg/1TabletOralHARRIS TEETER72036-982
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium trihydrate 20 mg/1Capsule, Delayed releaseOralINNOVUS PHARMACEUTICALS, INC.57483-900
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralYYBA CORP73581-013
EsomeprazoleEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralSafeway, Inc.21130-926
Esomeprazoleesomeprazole magnesiumEsomeprazole magnesium 20 mg/1Capsule, Delayed releaseOralCVS51316-715

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