What is NDC 64380-760?

64380-760 is the product NDC for Acarbose, Acarbose 100 mg/1 tablet, listed with the FDA by Strides Pharma Science Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

Strides Pharma Science Limited, NDC labeler code 64380. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Acarbose NDC 64380-760 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)64380-760Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64380-0760Add 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 NDC	11-digit (billing)	Package	Copy
64380-760-06	64380076006	100 TABLET in 1 BOTTLE, PLASTIC (64380-760-06)Marketed from Dec 10, 2016

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 — 100 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Strides Pharma Science LimitedNDC labeler code 64380
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090912
Marketing start: Dec 10, 2016
Listing expires: Dec 31, 2027
Other FDA classes: alpha Glucosidase Inhibitors (Mechanism)
Identifiers: Product ID 64380-760_dad62dcf-e1fe-4982-aece-136f46269185SPL ID dad62dcf-e1fe-4982-aece-136f46269185SPL set ID 656769ee-e292-4950-83df-a38e6b1a9d6eRxCUI 199149, 199150, 200132UNII T58MSI464GUPC 0364380760061, 0364380759089, 0364380758068
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

N464380076006 followed by a unit qualifier and the quantity

Package 64380-0760-06. 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 Jul 15, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Acarbose Tablets 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 64380-760

What is NDC 64380-760?: 64380-760 is the product NDC for Acarbose, Acarbose 100 mg/1 tablet, listed with the FDA by Strides Pharma Science Limited. It has 1 package NDC, 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?: Strides Pharma Science Limited, NDC labeler code 64380. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Acarbose	Acarbose 25 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-147	23155-0147-0123155-0147-0523155-0147-10
Acarbose	Acarbose 50 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-148	23155-0148-0123155-0148-0523155-0148-10
Acarbose	Acarbose 100 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-149	23155-0149-0123155-0149-0523155-0149-10
Acarbose	Acarbose 25 mg/1	TabletOral	Chartwell RX, LLC	62135-453	62135-0453-90
Acarbose	Acarbose 50 mg/1	TabletOral	Chartwell RX, LLC	62135-454	62135-0454-90
Acarbose	Acarbose 100 mg/1	TabletOral	Chartwell RX, LLC	62135-455	62135-0455-90
Acarbose	Acarbose 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-9725	71335-9725-0171335-9725-0271335-9725-03
Acarbose	Acarbose 50 mg/1	TabletOral	Bryant Ranch Prepack	63629-5698	63629-5698-0163629-5698-0263629-5698-03
Acarbose	Acarbose 50 mg/1	TabletOral	Strides Pharma Science Limited	64380-759	64380-0759-06
Acarbose	Acarbose 25 mg/1	TabletOral	Strides Pharma Science Limited	64380-758	64380-0758-06

All 17 Acarbose NDCs

Other NDCs under ANDA 090912

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

FDA NDC Directory listings under ANDA 090912
Product	Strength	Form · route	Labeler	Product NDC
Acarbose	Acarbose 50 mg/1	TabletOral	Bryant Ranch Prepack	63629-5698
Acarbose	Acarbose 25 mg/1	TabletOral	Strides Pharma Science Limited	64380-758
Acarbose	Acarbose 50 mg/1	TabletOral	Strides Pharma Science Limited	64380-759