NDC codes

FDA NDC Directory
Product NDC (as listed)23155-147Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0147Add 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
23155-147-0123155014701100 TABLET in 1 BOTTLE (23155-147-01)Marketed from Apr 16, 2021
23155-147-0523155014705500 TABLET in 1 BOTTLE (23155-147-05)Marketed from Apr 16, 2021
23155-147-10231550147101000 TABLET in 1 BOTTLE (23155-147-10)Marketed from Apr 16, 2021

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)
Acarbose
Generic name (nonproprietary)
acarbose
Active ingredients
Acarbose — 25 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202271
Marketing start
Listing expires
Other FDA classes
alpha Glucosidase Inhibitors (Mechanism)
Identifiers
Product ID 23155-147_dc1b5c0e-cd6b-482e-9388-e9183ca499e9SPL ID dc1b5c0e-cd6b-482e-9388-e9183ca499e9SPL set ID 29939129-7d09-4c22-bf3e-491a8a97f4c4RxCUI 199149, 199150, 200132UNII T58MSI464G
Pharmacologic class
alpha-Glucosidase 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

N423155014701 followed by a unit qualifier and the quantity

Package 23155-0147-01. 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)

INDICATIONS AND USAGE Acarbose tablets, USP are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-147

What is NDC 23155-147?
23155-147 is the product NDC for Acarbose, Acarbose 25 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Acarbose.
What is the active ingredient?
Acarbose.
Who is the labeler?
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acarbose?
16 other product NDCs are listed under this name. See all Acarbose 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 Acarbose NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AcarboseAcarbose 50 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-14823155-0148-0123155-0148-0523155-0148-10
AcarboseAcarbose 100 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-14923155-0149-0123155-0149-0523155-0149-10
AcarboseAcarbose 25 mg/1TabletOralChartwell RX, LLC62135-45362135-0453-90
AcarboseAcarbose 50 mg/1TabletOralChartwell RX, LLC62135-45462135-0454-90
AcarboseAcarbose 100 mg/1TabletOralChartwell RX, LLC62135-45562135-0455-90
AcarboseAcarbose 50 mg/1TabletOralBryant Ranch Prepack71335-972571335-9725-0171335-9725-0271335-9725-03
AcarboseAcarbose 50 mg/1TabletOralBryant Ranch Prepack63629-569863629-5698-0163629-5698-0263629-5698-03
AcarboseAcarbose 50 mg/1TabletOralStrides Pharma Science Limited64380-75964380-0759-06
AcarboseAcarbose 100 mg/1TabletOralStrides Pharma Science Limited64380-76064380-0760-06
AcarboseAcarbose 25 mg/1TabletOralStrides Pharma Science Limited64380-75864380-0758-06

All 17 Acarbose NDCs

Other NDCs under ANDA 202271

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

FDA NDC Directory listings under ANDA 202271
ProductStrengthForm · routeLabelerProduct NDC
AcarboseAcarbose 50 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-148
AcarboseAcarbose 100 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-149
AcarboseAcarbose 25 mg/1TabletOralChartwell RX, LLC62135-453
AcarboseAcarbose 50 mg/1TabletOralChartwell RX, LLC62135-454
AcarboseAcarbose 100 mg/1TabletOralChartwell RX, LLC62135-455
AcarboseAcarbose 50 mg/1TabletOralBryant Ranch Prepack71335-9725

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