What is NDC 0093-9364?

0093-9364 is the product NDC for Glyburide, Glyburide 5 mg/1 tablet, listed with the FDA by TEVA Pharmaceuticals USA Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.

TEVA Pharmaceuticals USA Inc, NDC labeler code 0093. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Glyburide NDC 0093-9364 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0093-9364Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00093-9364Add 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
0093-9364-01	0009393640100093936401	100 TABLET in 1 BOTTLE (0093-9364-01)Marketed from May 1, 1984
0093-9364-05	0009393640500093936405	500 TABLET in 1 BOTTLE (0093-9364-05)Marketed from May 1, 1984
0093-9364-10	0009393641000093936410	1000 TABLET in 1 BOTTLE (0093-9364-10)Marketed from May 1, 1984

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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: TEVA Pharmaceuticals USA IncNDC labeler code 0093
Product type: Prescription drug
Marketing category: NDA authorized genericApplication NDA 017532
Marketing start: May 1, 1984
Listing expires: Dec 31, 2026
Other FDA classes: Sulfonylurea Compounds (Chemical structure)
Identifiers: Product ID 0093-9364_84b83205-8813-494e-933e-a70697393744SPL ID 84b83205-8813-494e-933e-a70697393744SPL set ID 50d16f1d-c814-4411-8749-62561321ecceRxCUI 197737, 310534, 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

N400093936401 followed by a unit qualifier and the quantity

Package 00093-9364-01. 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 Jul 1, 2021.

Indications (excerpt from the label)

INDICATIONS AND USAGE Glyburide 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 0093-9364

What is NDC 0093-9364?: 0093-9364 is the product NDC for Glyburide, Glyburide 5 mg/1 tablet, listed with the FDA by TEVA Pharmaceuticals USA Inc. It has 3 package NDCs, 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?: TEVA Pharmaceuticals USA Inc, NDC labeler code 0093. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Glyburide	Glyburide 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4073	68788-4073-0168788-4073-0368788-4073-06+1 more
Glyburide	Glyburide 2.5 mg/1	TabletOral	Coupler LLC	67046-1620	67046-1620-03
Glyburide	Glyburide 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4035	70518-4035-0070518-4035-01
Glyburide	Glyburide 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8508	68788-8508-0168788-8508-0368788-8508-06+1 more
Glyburide	Glyburide 2.5 mg/1	TabletOral	REMEDYREPACK INC.	70518-3504	70518-3504-0070518-3504-01
Glyburide	Glyburide 5 mg/1	TabletOral	A-S Medication Solutions	50090-6196	50090-6196-0050090-6196-0150090-6196-02+2 more
Glyburide	Glyburide 2.5 mg/1	TabletOral	A-S Medication Solutions	50090-7408	50090-7408-0050090-7408-02
Glyburide	Glyburide 5 mg/1	TabletOral	A-S Medication Solutions	50090-7859	50090-7859-00
Glyburide	Glyburide 5 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3452	68071-3452-0368071-3452-06
Glyburide	Glyburide 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-2771	71335-2771-0171335-2771-0271335-2771-03+3 more

All 52 Glyburide NDCs

Other NDCs under NDA 017532

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

FDA NDC Directory listings under NDA 017532
Product	Strength	Form · route	Labeler	Product NDC
Glyburide	Glyburide 2.5 mg/1	TabletOral	TEVA Pharmaceuticals USA Inc	0093-9433
Glyburide	Glyburide 1.25 mg/1	TabletOral	TEVA Pharmaceuticals USA Inc	0093-9477