NDC codes

FDA NDC Directory
Product NDC (as listed)71335-0150Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-0150Add 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
71335-0150-17133501500130 TABLET in 1 BOTTLE (71335-0150-1)Marketed from Sep 4, 2018
71335-0150-271335015002120 TABLET in 1 BOTTLE (71335-0150-2)Marketed from Jan 28, 2025
71335-0150-371335015003100 TABLET in 1 BOTTLE (71335-0150-3)Marketed from Jan 28, 2025
71335-0150-47133501500460 TABLET in 1 BOTTLE (71335-0150-4)Marketed from Jul 23, 2018
71335-0150-57133501500590 TABLET in 1 BOTTLE (71335-0150-5)Marketed from May 23, 2018
71335-0150-671335015006180 TABLET in 1 BOTTLE (71335-0150-6)Marketed from Feb 12, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
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 71335-0150_5e1bb26d-3543-48d5-9a08-c07f5dd5a688SPL ID 5e1bb26d-3543-48d5-9a08-c07f5dd5a688SPL set ID 05341afe-5b7a-462a-a196-689cb09f83fcRxCUI 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

N471335015001 followed by a unit qualifier and the quantity

Package 71335-0150-01. 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

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

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