NDC codes

FDA NDC Directory
Product NDC (as listed)68071-4223Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-4223Add 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
68071-4223-3680714223036807142230330 TABLET in 1 BOTTLE (68071-4223-3)Marketed from Jan 11, 2018
68071-4223-6680714223066807142230660 TABLET in 1 BOTTLE (68071-4223-6)Marketed from Sep 14, 2026
68071-4223-86807142230868071422308180 TABLET in 1 BOTTLE (68071-4223-8)Marketed from Jan 13, 2026
68071-4223-9680714223096807142230990 TABLET in 1 BOTTLE (68071-4223-9)Marketed from Jan 11, 2018

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
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
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 68071-4223_5b75f1f3-0bc0-31ab-e063-6394a90a1f5dSPL ID 5b75f1f3-0bc0-31ab-e063-6394a90a1f5d
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

N468071422303 followed by a unit qualifier and the quantity

Package 68071-4223-03. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 68071-4223

What is NDC 68071-4223?
68071-4223 is the product NDC for Glipizide, Glipizide 5 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 4 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?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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 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 10 mg/1TabletOralCoupler LLC67046-0367
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4232

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