NDC codes

FDA NDC Directory
Product NDC (as listed)60760-794Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60760-0794Add 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
60760-794-30607600794306076007943030 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-794-30)Marketed from Jun 12, 2024

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 — 5 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
St. Mary's Medical Park PharmacyNDC labeler code 60760
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206928
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 60760-794_54ddfc18-60c8-38cb-e063-6394a90afb2cSPL ID 54ddfc18-60c8-38cb-e063-6394a90afb2cSPL set ID 1b2ef6e2-5e7c-761e-e063-6294a90addd0RxCUI 314006UNII 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

N460760079430 followed by a unit qualifier and the quantity

Package 60760-0794-30. 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)

Glipizide extended-release tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Glipizide extended-release tablets is a sulfonylurea indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus Limitations of Use: Not for treatment of type 1 diabetes or diabetic ketoacidosis 1.1 Limitations of Use Glipizide extended-release tablets are not recommended for the treatment of type 1 diabetes mellitus or diabetic ketoacidosis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60760-794

What is NDC 60760-794?
60760-794 is the product NDC for Glipizide, Glipizide 5 mg/1 tablet, extended release, listed with the FDA by St. Mary's Medical Park Pharmacy. It has 1 package NDC, 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?
St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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 206928

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

FDA NDC Directory listings under ANDA 206928
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6746
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6765
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralAurobindo Pharma Limited59651-781
GlipizideGlipizide 2.5 mg/1Tablet, Extended releaseOralAmerican Health Packaging60687-768
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralAmerican Health Packaging60687-881
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-793
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3898
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-4128
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2353
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-9742
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-2614
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC82868-025
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC82868-035

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