NDC codes

FDA NDC Directory
Product NDC (as listed)71335-9614Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-9614Add 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
71335-9614-17133596140160 TABLET in 1 BOTTLE (71335-9614-1)Marketed from Jan 23, 2023
71335-9614-27133596140230 TABLET in 1 BOTTLE (71335-9614-2)Marketed from Apr 13, 2023
71335-9614-371335961403100 TABLET in 1 BOTTLE (71335-9614-3)Marketed from Aug 26, 2026
71335-9614-471335961404120 TABLET in 1 BOTTLE (71335-9614-4)Marketed from Aug 26, 2026
71335-9614-57133596140590 TABLET in 1 BOTTLE (71335-9614-5)Marketed from Jan 19, 2023
71335-9614-67133596140620 TABLET in 1 BOTTLE (71335-9614-6)Marketed from Aug 26, 2026
71335-9614-771335961407180 TABLET in 1 BOTTLE (71335-9614-7)Marketed from Mar 17, 2023

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
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 71335-9614_7d34b9a2-5eab-4093-aec0-29c8f2825f36SPL ID 7d34b9a2-5eab-4093-aec0-29c8f2825f36SPL set ID a59e2aaf-692c-4696-817b-3fed7a9dc52cRxCUI 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

N471335961401 followed by a unit qualifier and the quantity

Package 71335-9614-01. 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)

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 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3548
GlipizideGlipizide 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0437
GlipizideGlipizide 5 mg/1TabletOralGolden State Medical Supply, Inc.51407-620
GlipizideGlipizide 10 mg/1TabletOralGolden State Medical Supply, Inc.51407-621
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack72162-2215
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7405
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7404
GlipizideGlipizide 5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-315
GlipizideGlipizide 10 mg/1TabletOralANI Pharmaceuticals, Inc.62559-316
GlipizideGlipizide 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-668
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-2520
GlipizideGlipizide 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-680

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