NDC codes

FDA NDC Directory
Product NDC (as listed)68788-7856Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-7856Add 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
68788-7856-168788785601100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-1)Marketed from Jan 29, 2021
68788-7856-36878878560330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-3)Marketed from Jan 29, 2021
68788-7856-66878878560660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-6)Marketed from Jan 29, 2021
68788-7856-96878878560990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-9)Marketed from Jan 29, 2021

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, Film coated, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204720
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 68788-7856_b7b2f928-04f2-453f-afad-553beea19c0eSPL ID b7b2f928-04f2-453f-afad-553beea19c0eSPL set ID 548c1f50-dbf0-49cc-b58b-fcc5937affa8RxCUI 315107UNII 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

N468788785601 followed by a unit qualifier and the quantity

Package 68788-7856-01. 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)

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 tablet 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)

Other NDCs under ANDA 204720

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

FDA NDC Directory listings under ANDA 204720
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 10 mg/1Tablet, Film coated, Extended releaseOralREMEDYREPACK INC.70518-1848
GlipizideGlipizide 10 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-5806
GlipizideGlipizide 10 mg/1Tablet, Film coated, Extended releaseOralNorthwind Health Company, LLC51655-966
GlipizideGlipizide 2.5 mg/1Tablet, Film coated, Extended releaseOralPreferred Pharmaceuticals Inc.68788-8487
GlipizideGlipizide 5 mg/1Tablet, Film coated, Extended releaseOralBryant Ranch Prepack71335-1031
GlipizideGlipizide 2.5 mg/1Tablet, Film coated, Extended releaseOralBryant Ranch Prepack71335-1042
GlipizideGlipizide 5 mg/1Tablet, Film coated, Extended releaseOralREMEDYREPACK INC.70518-1063
GlipizideGlipizide 2.5 mg/1Tablet, Film coated, Extended releaseOralREMEDYREPACK INC.70518-2308
GlipizideGlipizide 10 mg/1Tablet, Film coated, Extended releaseOralBryant Ranch Prepack71335-1130
GlipizideGlipizide 2.5 mg/1Tablet, Film coated, Extended releaseOralRising Pharma Holdings, Inc.64980-279
GlipizideGlipizide 5 mg/1Tablet, Film coated, Extended releaseOralRising Pharma Holdings, Inc.64980-280
GlipizideGlipizide 10 mg/1Tablet, Film coated, Extended releaseOralRising Pharma Holdings, Inc.64980-281
GlipizideGlipizide 5 mg/1Tablet, Film coated, Extended releaseOralNorthwind Health Company, LLC51655-337
GlipizideGlipizide 5 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-5040

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