NDC codes

FDA NDC Directory
Product NDC (as listed)68788-4178Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68788-4178Add 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
68788-4178-16878841780168788417801100 TABLET in 1 BOTTLE (68788-4178-1)Marketed from Jul 31, 2026
68788-4178-3687884178036878841780330 TABLET in 1 BOTTLE (68788-4178-3)Marketed from Jul 31, 2026
68788-4178-6687884178066878841780660 TABLET in 1 BOTTLE (68788-4178-6)Marketed from Jul 31, 2026
68788-4178-86878841780868788417808180 TABLET in 1 BOTTLE (68788-4178-8)Marketed from Jul 31, 2026
68788-4178-9687884178096878841780990 TABLET in 1 BOTTLE (68788-4178-9)Marketed from Jul 31, 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 — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074378
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 68788-4178_e0de2d19-b24b-46af-a10e-0b78c51350a4SPL ID e0de2d19-b24b-46af-a10e-0b78c51350a4SPL set ID e0de2d19-b24b-46af-a10e-0b78c51350a4RxCUI 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

N468788417801 followed by a unit qualifier and the quantity

Package 68788-4178-01. 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 68788-4178

What is NDC 68788-4178?
68788-4178 is the product NDC for Glipizide, Glipizide 5 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 package NDCs, 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?
Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 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
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-402068788-4020-0168788-4020-0368788-4020-06+2 more

All 136 Glipizide NDCs

Other NDCs under ANDA 074378

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

FDA NDC Directory listings under ANDA 074378
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 5 mg/1TabletOralProficient Rx LP82804-959
GlipizideGlipizide 10 mg/1TabletOralProficient Rx LP82804-960
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-3133
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-8098
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4061
GlipizideGlipizide 5 mg/1TabletOralOxford Pharmaceuticals, LLC69584-309
GlipizideGlipizide 10 mg/1TabletOralOxford Pharmaceuticals, LLC69584-310
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-5326
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-8178

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