NDC codes

FDA NDC Directory
Product NDC (as listed)55289-806Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55289-0806Add 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
55289-806-935528908069355289080693180 TABLET in 1 BOTTLE, PLASTIC (55289-806-93)Marketed from Feb 27, 1995

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
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 55289
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074223
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 55289-806_419b3f40-b99c-8778-e063-6294a90ae23aSPL ID 419b3f40-b99c-8778-e063-6294a90ae23aSPL set ID c829b7bf-1a12-44b2-b5ce-fd44a1f0d333RxCUI 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

N455289080693 followed by a unit qualifier and the quantity

Package 55289-0806-93. 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 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)

About NDC 55289-806

What is NDC 55289-806?
55289-806 is the product NDC for Glipizide, Glipizide 5 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Glipizide.
What is the active ingredient?
Glipizide.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 55289. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Glipizide?
135 other product NDCs are listed under this name. See all Glipizide NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Glipizide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
GlipizideGlipizide 5 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-11711788-0117-0111788-0117-0511788-0117-10
GlipizideGlipizide 10 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-11811788-0118-00
GlipizideGlipizide 2.5 mg/1TabletOralAiPing Pharmaceutical, Inc.11788-12011788-0120-0111788-0120-0511788-0120-10
GlipizideGlipizide 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-57972789-0579-3072789-0579-6072789-0579-86+3 more
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-58072789-0580-3072789-0580-6072789-0580-86+3 more
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-417868788-4178-0168788-4178-0368788-4178-06+2 more
GlipizideGlipizide 10 mg/1TabletOralCoupler LLC67046-036767046-0367-03
GlipizideGlipizide 5 mg/1TabletOralCoupler LLC67046-023667046-0236-03
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-406168788-4061-0168788-4061-0368788-4061-06+2 more
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-401768788-4017-0168788-4017-0368788-4017-06+2 more

All 136 Glipizide NDCs

Other NDCs under ANDA 074223

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

FDA NDC Directory listings under ANDA 074223
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 5 mg/1TabletOralActavis Pharma, Inc.0591-0460
GlipizideGlipizide 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8407
GlipizideGlipizide 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8408
GlipizideGlipizide 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC43353-207
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-0503
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-6473
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-6996
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7908
GlipizideGlipizide 10 mg/1TabletOralNorthwind Health Company, LLC51655-810
GlipizideGlipizide 10 mg/1TabletOralProficient Rx LP63187-811
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack63629-1398
GlipizideGlipizide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4085
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4124
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4643
GlipizideGlipizide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4939
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc..68788-8138
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8512

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