NDC codes

FDA NDC Directory
Product NDC (as listed)50090-6849Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-6849Add 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
50090-6849-05009068490090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6849-0)Marketed from Nov 29, 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, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203499
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 50090-6849_6fd6db61-c772-4909-a782-2f7dcd296c89SPL ID 6fd6db61-c772-4909-a782-2f7dcd296c89SPL set ID 15308fc4-11e3-4cd5-8f04-ab8e3433cc7dRxCUI 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

N450090684900 followed by a unit qualifier and the quantity

Package 50090-6849-00. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Glipizide extended-release tablets 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. Glipizide extended-release tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. 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 203499

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

FDA NDC Directory listings under ANDA 203499
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 2.5 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3645
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3896
GlipizideGlipizide 2.5 mg/1Tablet, Extended releaseOralNorthstar Rx LLC.16714-894
GlipizideGlipizide 5 mg/1Tablet, Extended releaseOralNorthstar Rx LLC.16714-895
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralNorthstar Rx LLC.16714-896
GlipizideGlipizide 10 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-6848

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