NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4085Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4085Add 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
68071-4085-36807140850330 TABLET in 1 BOTTLE (68071-4085-3)Marketed from Sep 7, 2017
68071-4085-66807140850660 TABLET in 1 BOTTLE (68071-4085-6)Marketed from Sep 7, 2017
68071-4085-868071408508180 TABLET in 1 BOTTLE (68071-4085-8)Marketed from Sep 7, 2017
68071-4085-96807140850990 TABLET in 1 BOTTLE (68071-4085-9)Marketed from Sep 7, 2017

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 — 5 mg/1
Dosage form
Tablet
Route
Oral
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 68071-4085_1d8e2506-3bca-bff2-e063-6294a90a6e5aSPL ID 1d8e2506-3bca-bff2-e063-6294a90a6e5aSPL set ID 589dc76d-c347-0589-e053-2991aa0a2520RxCUI 310490UNII X7WDT95N5CUPC 0368071408560
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

N468071408503 followed by a unit qualifier and the quantity

Package 68071-4085-03. 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 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 10 mg/1TabletOralA-S Medication Solutions50090-6996
GlipizideGlipizide 5 mg/1TabletOralActavis Pharma, Inc.0591-0460
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7908
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8512
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc..68788-8138
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4643
GlipizideGlipizide 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC43353-207
GlipizideGlipizide 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8407
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-6473
GlipizideGlipizide 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8408
GlipizideGlipizide 10 mg/1TabletOralActavis Pharma, Inc.0591-0461
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack63629-1398
GlipizideGlipizide 10 mg/1TabletOralProficient Rx LP63187-811
GlipizideGlipizide 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.55289-806
GlipizideGlipizide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4939
GlipizideGlipizide 10 mg/1TabletOralNorthwind Health Company, LLC51655-810
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4124

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