NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5806Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5806Add 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
50090-5806-05009058060030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5806-0)Marketed from Oct 15, 2021
50090-5806-15009058060160 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5806-1)Marketed from Oct 15, 2021
50090-5806-25009058060290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5806-2)Marketed from Oct 15, 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 50090-5806_50844523-1657-40e7-ba83-320b4b91bc6cSPL ID 50844523-1657-40e7-ba83-320b4b91bc6cSPL set ID 4982f018-c53c-48ec-a4e8-4834228bcf2cRxCUI 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

N450090580600 followed by a unit qualifier and the quantity

Package 50090-5806-00. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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 releaseOralPreferred Pharmaceuticals Inc.68788-7856
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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