NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3974Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3974Add 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
68071-3974-868071397408180 TABLET in 1 BOTTLE (68071-3974-8)Marketed from Jun 19, 2026
68071-3974-96807139740990 TABLET in 1 BOTTLE (68071-3974-9)Marketed from Mar 5, 2026

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
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214874
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 68071-3974_549ef654-60b9-05bb-e063-6294a90a22b8SPL ID 549ef654-60b9-05bb-e063-6294a90a22b8SPL set ID 4c4dfe64-d1c5-65ec-e063-6394a90aead5RxCUI 310488UNII X7WDT95N5CUPC 0368071397499
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

N468071397408 followed by a unit qualifier and the quantity

Package 68071-3974-08. 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 214874

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

FDA NDC Directory listings under ANDA 214874
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 15 mg/1TabletOralAdvagen Pharma Limited72888-231
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-463
GlipizideGlipizide 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-464
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-510
GlipizideGlipizide 5 mg/1TabletOralProficient Rx LP82804-174
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4020
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4017
GlipizideGlipizide 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0549
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7734
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7735
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7755
GlipizideGlipizide 2.5 mg/1TabletOralTruPharma LLC52817-385
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7756
GlipizideGlipizide 5 mg/1TabletOralAdvagen Pharma Limited72888-116
GlipizideGlipizide 2.5 mg/1TabletOralAdvagen Pharma Limited72888-115
GlipizideGlipizide 10 mg/1TabletOralAdvagen Pharma Limited72888-117
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-2528
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack71335-2540

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