Glyburide NDC 66267-103

NDC codes

FDA NDC Directory

Product NDC (as listed)66267-103Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66267-0103Add 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
66267-103-30	66267010330	30 TABLET in 1 BOTTLE (66267-103-30)Marketed from Oct 6, 2016
66267-103-60	66267010360	60 TABLET in 1 BOTTLE (66267-103-60)Marketed from Oct 6, 2016
66267-103-90	66267010390	90 TABLET in 1 BOTTLE (66267-103-90)Marketed from Oct 6, 2016
66267-103-91	66267010391	120 TABLET in 1 BOTTLE (66267-103-91)Marketed from Oct 6, 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): Glyburide
Generic name (nonproprietary): glyburide
Active ingredients: Glyburide — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090937
Marketing start: Oct 5, 2010
Listing expires: Dec 31, 2026
Other FDA classes: Sulfonylurea Compounds (Chemical structure)
Identifiers: Product ID 66267-103_1f98dd6f-ab6b-c359-e063-6394a90af09eSPL ID 1f98dd6f-ab6b-c359-e063-6394a90af09eSPL set ID 3e354b4d-70e4-5089-e054-00144ff88e88RxCUI 310537UNII 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

N466267010330 followed by a unit qualifier and the quantity

Package 66267-0103-30. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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
Product	Strength	Form · route	Labeler	Product NDC
Glyburide	Glyburide 2.5 mg/1	TabletOral	A-S Medication Solutions	50090-5776
Glyburide	Glyburide 5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5030
Glyburide	Glyburide 5 mg/1	TabletOral	A-S Medication Solutions	50090-0495
Glyburide	Glyburide 2.5 mg/1	TabletOral	Proficient Rx LP	63187-659
Glyburide	Glyburide 5 mg/1	TabletOral	Northwind Health Company, LLC	51655-492
Glyburide	Glyburide 5 mg/1	TabletOral	Proficient Rx LP	63187-667
Glyburide	Glyburide 5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5215
Glyburide	Glyburide 5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4695
Glyburide	Glyburide 2.5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-5217
Glyburide	Glyburide 2.5 mg/1	TabletOral	Chartwell RX, LLC	62135-584
Glyburide	Glyburide 1.25 mg/1	TabletOral	Chartwell RX, LLC	62135-583
Glyburide	Glyburide 2.5 mg/1	TabletOral	Northwind Health Company, LLC	51655-659
Glyburide	Glyburide 5 mg/1	TabletOral	Chartwell RX, LLC	62135-585
Glyburide	Glyburide 2.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0069
Glyburide	Glyburide 2.5 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-057
Glyburide	Glyburide 1.25 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-056
Glyburide	Glyburide 5 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-058
Glyburide	Glyburide 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-0150