NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0437Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0437Add 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
80425-0437-1804250437018042504370130 TABLET in 1 BOTTLE (80425-0437-1)Marketed from Sep 3, 2024
80425-0437-2804250437028042504370260 TABLET in 1 BOTTLE (80425-0437-2)Marketed from Sep 3, 2024
80425-0437-3804250437038042504370390 TABLET in 1 BOTTLE (80425-0437-3)Marketed from Sep 3, 2024

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 074497
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 80425-0437_213c486b-f952-bffc-e063-6394a90a164eSPL ID 213c486b-f952-bffc-e063-6394a90a164eSPL set ID 213c4e61-9bb7-9d1b-e063-6394a90a7339RxCUI 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

N480425043701 followed by a unit qualifier and the quantity

Package 80425-0437-01. 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 USP 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 80425-0437

What is NDC 80425-0437?
80425-0437 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 074497

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

FDA NDC Directory listings under ANDA 074497
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7404
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7405
GlipizideGlipizide 5 mg/1TabletOralGolden State Medical Supply, Inc.51407-620
GlipizideGlipizide 10 mg/1TabletOralGolden State Medical Supply, Inc.51407-621
GlipizideGlipizide 5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-315
GlipizideGlipizide 10 mg/1TabletOralANI Pharmaceuticals, Inc.62559-316
GlipizideGlipizide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3548
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-2520
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack71335-9614
GlipizideGlipizide 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-668
GlipizideGlipizide 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-680
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack72162-2215

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