NDC codes

FDA NDC Directory
Product NDC (as listed)52817-385Labeler and product segments. Claims need a package NDC.
Product NDC at billing width52817-0385Add 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
52817-385-105281703851052817038510100 TABLET in 1 BOTTLE (52817-385-10)Marketed from Oct 3, 2023
52817-385-505281703855052817038550500 TABLET in 1 BOTTLE (52817-385-50)Marketed from Oct 3, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 — 2.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
TruPharma LLCNDC labeler code 52817
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 52817-385_076b74ec-ead5-781c-e063-6394a90ab362SPL ID 076b74ec-ead5-781c-e063-6394a90ab362SPL set ID 95ea4c96-84b9-4515-9494-a93d26820f70RxCUI 379804UNII X7WDT95N5CUPC 0352817385109, 0352817385505
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

N452817038510 followed by a unit qualifier and the quantity

Package 52817-0385-10. 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 52817-385

What is NDC 52817-385?
52817-385 is the product NDC for Glipizide, Glipizide 2.5 mg/1 tablet, listed with the FDA by TruPharma LLC. It has 2 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?
TruPharma LLC, NDC labeler code 52817. 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 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 10 mg/1TabletOralA-S Medication Solutions50090-7734
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7735
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7755
GlipizideGlipizide 5 mg/1TabletOralA-S Medication Solutions50090-7756
GlipizideGlipizide 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3974
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4017
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-4020
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-2528
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack71335-2540
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 2.5 mg/1TabletOralAdvagen Pharma Limited72888-115
GlipizideGlipizide 5 mg/1TabletOralAdvagen Pharma Limited72888-116
GlipizideGlipizide 10 mg/1TabletOralAdvagen Pharma Limited72888-117
GlipizideGlipizide 15 mg/1TabletOralAdvagen Pharma Limited72888-231
GlipizideGlipizide 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0549
GlipizideGlipizide 5 mg/1TabletOralProficient Rx LP82804-174

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