NDC codes

FDA NDC Directory
Product NDC (as listed)51407-620Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51407-0620Add 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
51407-620-10514070620101000 TABLET in 1 BOTTLE (51407-620-10)Marketed from Jan 12, 2022

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
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 51407-620_57a03823-566b-7ef2-e063-6394a90af4e6SPL ID 57a03823-566b-7ef2-e063-6394a90af4e6SPL set ID d91d021f-f644-eac7-e053-2995a90a81c4RxCUI 310488, 310490UNII 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

N451407062010 followed by a unit qualifier and the quantity

Package 51407-0620-10. 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 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/1TabletOralBryant Ranch Prepack71335-9614
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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Glipizide NDC 51407-620 | Med-Code