NDC codes

FDA NDC Directory
Product NDC (as listed)69584-310Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69584-0310Add 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
69584-310-096958403100990 TABLET in 1 BOTTLE (69584-310-09)Marketed from Sep 18, 2026
69584-310-1069584031010100 TABLET in 1 BOTTLE (69584-310-10)Marketed from May 1, 2025
69584-310-1869584031018180 TABLET in 1 BOTTLE (69584-310-18)Marketed from Sep 18, 2026
69584-310-3669584031036360 TABLET in 1 BOTTLE (69584-310-36)Marketed from Sep 18, 2026
69584-310-5069584031050500 TABLET in 1 BOTTLE (69584-310-50)Marketed from May 1, 2025
69584-310-90695840310901000 TABLET in 1 BOTTLE (69584-310-90)Marketed from May 1, 2025

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 — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074378
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 69584-310_02a8d094-c2c7-436e-b77e-9889345be1f2SPL ID 02a8d094-c2c7-436e-b77e-9889345be1f2
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

N469584031009 followed by a unit qualifier and the quantity

Package 69584-0310-09. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 074378

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

FDA NDC Directory listings under ANDA 074378
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 5 mg/1TabletOralProficient Rx LP82804-959
GlipizideGlipizide 10 mg/1TabletOralProficient Rx LP82804-960
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4178
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-3133
GlipizideGlipizide 5 mg/1TabletOralOxford Pharmaceuticals, LLC69584-309
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4061

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