NDC codes

FDA NDC Directory
Product NDC (as listed)67046-0367Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-0367Add 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
67046-0367-3670460367036704603670330 TABLET in 1 BLISTER PACK (67046-0367-3)Marketed from Jun 10, 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
Labeler
Coupler LLCNDC labeler code 67046
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075795
Marketing start
Listing expires
Other FDA classes
Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 67046-0367_53e67073-8a11-c8b0-e063-6294a90a90ccSPL ID 53e67073-8a11-c8b0-e063-6294a90a90ccSPL set ID 53e650f1-f755-e3ad-e063-6294a90ae309RxCUI 310488UNII 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

N467046036703 followed by a unit qualifier and the quantity

Package 67046-0367-03. 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

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 67046-0367

What is NDC 67046-0367?
67046-0367 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by Coupler LLC. 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?
Coupler LLC, NDC labeler code 67046. 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 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 075795

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

FDA NDC Directory listings under ANDA 075795
ProductStrengthForm · routeLabelerProduct NDC
GlipizideGlipizide 5 mg/1TabletOralMajor Pharmaceuticals0904-6637
GlipizideGlipizide 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-861
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-0502
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-0505
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-6975
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7197
GlipizideGlipizide 5 mg/1TabletOralAvPAK50268-361
GlipizideGlipizide 10 mg/1TabletOralAvPAK50268-362
GlipizideGlipizide 10 mg/1TabletOralNorthwind Health Company, LLC51655-106
GlipizideGlipizide 5 mg/1TabletOralNorthwind Health Company, LLC51655-180
GlipizideGlipizide 5 mg/1TabletOralCardinal Health 107, LLC55154-7987
GlipizideGlipizide 5 mg/1TabletOralApotex Corp.60505-0141
GlipizideGlipizide 10 mg/1TabletOralApotex Corp.60505-0142
GlipizideGlipizide 5 mg/1TabletOralAmerican Health Packaging60687-690
GlipizideGlipizide 10 mg/1TabletOralAmerican Health Packaging60687-701
GlipizideGlipizide 10 mg/1TabletOralProficient Rx LP63187-993
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.66267-099
GlipizideGlipizide 5 mg/1TabletOralCoupler LLC67046-0236
GlipizideGlipizide 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4223
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4232

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