NDC codes

FDA NDC Directory
Product NDC (as listed)51655-659Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0659Add 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
51655-659-52516550659525165506595230 TABLET in 1 BOTTLE, PLASTIC (51655-659-52)Marketed from Mar 23, 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)
Glyburide
Generic name (nonproprietary)
glyburide
Active ingredients
Glyburide — 2.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Northwind Health Company, LLCNDC labeler code 51655
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090937
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 51655-659_4b8239f0-5467-fb1e-e063-6294a90a7679SPL ID 4b8239f0-5467-fb1e-e063-6294a90a7679SPL set ID db47a517-f8bb-136f-e053-2a95a90ad8c5RxCUI 310534UNII SX6K58TVWC
Pharmacologic class
Sulfonylurea

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

N451655065952 followed by a unit qualifier and the quantity

Package 51655-0659-52. 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 Glyburide tablets, USP is 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 51655-659

What is NDC 51655-659?
51655-659 is the product NDC for Glyburide, Glyburide 2.5 mg/1 tablet, listed with the FDA by Northwind Health Company, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Glyburide.
What is the active ingredient?
Glyburide.
Who is the labeler?
Northwind Health Company, LLC, NDC labeler code 51655. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Glyburide?
51 other product NDCs are listed under this name. See all Glyburide 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 Glyburide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
GlyburideGlyburide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-407368788-4073-0168788-4073-0368788-4073-06+1 more
GlyburideGlyburide 2.5 mg/1TabletOralCoupler LLC67046-162067046-1620-03
GlyburideGlyburide 5 mg/1TabletOralREMEDYREPACK INC.70518-403570518-4035-0070518-4035-01
GlyburideGlyburide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-850868788-8508-0168788-8508-0368788-8508-06+1 more
GlyburideGlyburide 2.5 mg/1TabletOralREMEDYREPACK INC.70518-350470518-3504-0070518-3504-01
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-619650090-6196-0050090-6196-0150090-6196-02+2 more
GlyburideGlyburide 2.5 mg/1TabletOralA-S Medication Solutions50090-740850090-7408-0050090-7408-02
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-785950090-7859-00
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-345268071-3452-0368071-3452-06
GlyburideGlyburide 5 mg/1TabletOralBryant Ranch Prepack71335-277171335-2771-0171335-2771-0271335-2771-03+3 more

All 52 Glyburide NDCs

Other NDCs under ANDA 090937

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

FDA NDC Directory listings under ANDA 090937
ProductStrengthForm · routeLabelerProduct NDC
GlyburideGlyburide 1.25 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-056
GlyburideGlyburide 2.5 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-057
GlyburideGlyburide 5 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-058
GlyburideGlyburide 5 mg/1TabletOralA-S Medication Solutions50090-0495
GlyburideGlyburide 2.5 mg/1TabletOralA-S Medication Solutions50090-5776
GlyburideGlyburide 5 mg/1TabletOralNorthwind Health Company, LLC51655-492
GlyburideGlyburide 1.25 mg/1TabletOralChartwell RX, LLC62135-583
GlyburideGlyburide 2.5 mg/1TabletOralChartwell RX, LLC62135-584
GlyburideGlyburide 5 mg/1TabletOralChartwell RX, LLC62135-585
GlyburideGlyburide 2.5 mg/1TabletOralProficient Rx LP63187-659
GlyburideGlyburide 5 mg/1TabletOralProficient Rx LP63187-667
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals, Inc.66267-103
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4695
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5030
GlyburideGlyburide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5215
GlyburideGlyburide 2.5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5217
GlyburideGlyburide 2.5 mg/1TabletOralBryant Ranch Prepack71335-0069
GlyburideGlyburide 5 mg/1TabletOralBryant Ranch Prepack71335-0150

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