What is NDC 69584-310?

69584-310 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by Oxford Pharmaceuticals, LLC. It has 6 package NDCs, shown above in 10- and 11-digit form.

Oxford Pharmaceuticals, LLC, NDC labeler code 69584. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Glipizide?

135 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Glipizide NDC 69584-310 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)69584-310Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69584-0310Add 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
69584-310-09	6958403100969584031009	90 TABLET in 1 BOTTLE (69584-310-09)Marketed from Sep 18, 2026
69584-310-10	6958403101069584031010	100 TABLET in 1 BOTTLE (69584-310-10)Marketed from May 1, 2025
69584-310-18	6958403101869584031018	180 TABLET in 1 BOTTLE (69584-310-18)Marketed from Sep 18, 2026
69584-310-36	6958403103669584031036	360 TABLET in 1 BOTTLE (69584-310-36)Marketed from Sep 18, 2026
69584-310-50	6958403105069584031050	500 TABLET in 1 BOTTLE (69584-310-50)Marketed from May 1, 2025
69584-310-90	6958403109069584031090	1000 TABLET in 1 BOTTLE (69584-310-90)Marketed from May 1, 2025

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): Glipizide
Generic name (nonproprietary): glipizide
Active ingredients: Glipizide — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Oxford Pharmaceuticals, LLCNDC labeler code 69584
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074378
Marketing start: May 1, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Sulfonylurea Compounds (Chemical structure)
Identifiers: Product ID 69584-310_02a8d094-c2c7-436e-b77e-9889345be1f2SPL ID 02a8d094-c2c7-436e-b77e-9889345be1f2
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

N469584031009 followed by a unit qualifier and the quantity

Package 69584-0310-09. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 69584-310

What is NDC 69584-310?: 69584-310 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by Oxford Pharmaceuticals, LLC. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Glipizide.
What is the active ingredient?: Glipizide.
Who is the labeler?: Oxford Pharmaceuticals, LLC, NDC labeler code 69584. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Glipizide?: 135 other product NDCs are listed under this name. See all Glipizide 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 Glipizide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Glipizide	Glipizide 5 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-117	11788-0117-0111788-0117-0511788-0117-10
Glipizide	Glipizide 10 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-118	11788-0118-00
Glipizide	Glipizide 2.5 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-120	11788-0120-0111788-0120-0511788-0120-10
Glipizide	Glipizide 5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-579	72789-0579-3072789-0579-6072789-0579-86+3 more
Glipizide	Glipizide 10 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-580	72789-0580-3072789-0580-6072789-0580-86+3 more
Glipizide	Glipizide 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4178	68788-4178-0168788-4178-0368788-4178-06+2 more
Glipizide	Glipizide 10 mg/1	TabletOral	Coupler LLC	67046-0367	67046-0367-03
Glipizide	Glipizide 5 mg/1	TabletOral	Coupler LLC	67046-0236	67046-0236-03
Glipizide	Glipizide 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4061	68788-4061-0168788-4061-0368788-4061-06+2 more
Glipizide	Glipizide 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4017	68788-4017-0168788-4017-0368788-4017-06+2 more

All 136 Glipizide NDCs

Other NDCs under ANDA 074378

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

FDA NDC Directory listings under ANDA 074378
Product	Strength	Form · route	Labeler	Product NDC
Glipizide	Glipizide 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4178
Glipizide	Glipizide 5 mg/1	TabletOral	Proficient Rx LP	82804-959
Glipizide	Glipizide 10 mg/1	TabletOral	Proficient Rx LP	82804-960
Glipizide	Glipizide 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-3133
Glipizide	Glipizide 10 mg/1	TabletOral	A-S Medication Solutions	50090-8098
Glipizide	Glipizide 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4061
Glipizide	Glipizide 5 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-309
Glipizide	Glipizide 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-5326
Glipizide	Glipizide 5 mg/1	TabletOral	A-S Medication Solutions	50090-8178