NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0549Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0549Add 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
80425-0549-1804250549018042505490130 TABLET in 1 BOTTLE (80425-0549-1)Marketed from Aug 29, 2025
80425-0549-2804250549028042505490260 TABLET in 1 BOTTLE (80425-0549-2)Marketed from Aug 29, 2025
80425-0549-3804250549038042505490390 TABLET in 1 BOTTLE (80425-0549-3)Marketed from Aug 29, 2025

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
Advanced Rx of Tennessee, LLCNDC labeler code 80425
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214874
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 80425-0549_3d87c932-9653-482e-e063-6294a90a3b84SPL ID 3d87c932-9653-482e-e063-6294a90a3b84SPL set ID 3d87cc75-7a0d-46a2-e063-6294a90a6d49RxCUI 310488UNII X7WDT95N5C
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

N480425054901 followed by a unit qualifier and the quantity

Package 80425-0549-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Glipizide tablets are 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 80425-0549

What is NDC 80425-0549?
80425-0549 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by Advanced Rx of Tennessee, LLC. It has 3 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?
Advanced Rx of Tennessee, LLC, NDC labeler code 80425. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
GlipizideGlipizide 5 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-11711788-0117-0111788-0117-0511788-0117-10
GlipizideGlipizide 10 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-11811788-0118-00
GlipizideGlipizide 2.5 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-12011788-0120-0111788-0120-0511788-0120-10
GlipizideGlipizide 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-57972789-0579-3072789-0579-6072789-0579-86+3 more
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-58072789-0580-3072789-0580-6072789-0580-86+3 more
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-417868788-4178-0168788-4178-0368788-4178-06+2 more
GlipizideGlipizide 10 mg/1TabletOralCoupler LLC67046-036767046-0367-03
GlipizideGlipizide 5 mg/1TabletOralCoupler LLC67046-023667046-0236-03
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-406168788-4061-0168788-4061-0368788-4061-06+2 more
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-401768788-4017-0168788-4017-0368788-4017-06+2 more

All 136 Glipizide NDCs

Other NDCs under ANDA 214874

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

FDA NDC Directory listings under ANDA 214874
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7734
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7735
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7755
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7756
GlipizideGlipizide 2.5 mg/1TabletOralTruPharma LLC52817-385
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3974
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4017
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4020
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-2528
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack71335-2540
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-463
GlipizideGlipizide 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-464
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-510
GlipizideGlipizide 2.5 mg/1TabletOralAdvagen Pharma Limited72888-115
GlipizideGlipizide 5 mg/1TabletOralAdvagen Pharma Limited72888-116
GlipizideGlipizide 10 mg/1TabletOralAdvagen Pharma Limited72888-117
GlipizideGlipizide 15 mg/1TabletOralAdvagen Pharma Limited72888-231
GlipizideGlipizide 5 mg/1TabletOralProficient Rx LP82804-174

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