What is NDC 50090-8098?

50090-8098 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 5 package NDCs, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. 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?

140 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 50090-8098 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-8098Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-8098Add 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
50090-8098-0	5009080980050090809800	30 TABLET in 1 BOTTLE (50090-8098-0)Marketed from Oct 5, 2026
50090-8098-1	5009080980150090809801	60 TABLET in 1 BOTTLE (50090-8098-1)Marketed from Oct 5, 2026
50090-8098-2	5009080980250090809802	100 TABLET in 1 BOTTLE (50090-8098-2)Marketed from Oct 5, 2026
50090-8098-5	5009080980550090809805	90 TABLET in 1 BOTTLE (50090-8098-5)Marketed from Oct 5, 2026
50090-8098-6	5009080980650090809806	180 TABLET in 1 BOTTLE (50090-8098-6)Marketed from Oct 5, 2026

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): Glipizide
Generic name (nonproprietary): glipizide
Active ingredients: Glipizide — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: A-S Medication SolutionsNDC labeler code 50090
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 50090-8098_f826e2b4-7382-4fc8-a96e-278a0334f5a1SPL ID f826e2b4-7382-4fc8-a96e-278a0334f5a1
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

N450090809800 followed by a unit qualifier and the quantity

Package 50090-8098-00. 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 50090-8098

What is NDC 50090-8098?: 50090-8098 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 5 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?: A-S Medication Solutions, NDC labeler code 50090. 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?: 140 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 10 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-118	11788-0118-00
Glipizide	Glipizide 5 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-117	11788-0117-00
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	11788-0118-0111788-0118-0511788-0118-10
Glipizide	Glipizide 2.5 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-120	11788-0120-0111788-0120-0511788-0120-10
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	PD-Rx Pharmaceuticals, Inc.	72789-579	72789-0579-3072789-0579-6072789-0579-86+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

All 141 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 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-5326
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	Preferred Pharmaceuticals Inc.	68788-4178
Glipizide	Glipizide 5 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-309
Glipizide	Glipizide 10 mg/1	TabletOral	Oxford Pharmaceuticals, LLC	69584-310
Glipizide	Glipizide 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-3133
Glipizide	Glipizide 10 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4061