NDC codes

FDA NDC Directory
Product NDC (as listed)70518-0579Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-0579Add 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
70518-0579-07051805790070518057900180 TABLET in 1 BOTTLE, PLASTIC (70518-0579-0)Marketed from Jun 20, 2017
70518-0579-1705180579017051805790130 TABLET in 1 BLISTER PACK (70518-0579-1)Marketed from Apr 25, 2018
70518-0579-2705180579027051805790290 TABLET in 1 BOTTLE, PLASTIC (70518-0579-2)Marketed from Jul 31, 2018
70518-0579-37051805790370518057903100 TABLET in 1 BOTTLE, PLASTIC (70518-0579-3)Marketed from Sep 5, 2018
70518-0579-7705180579077051805790730 TABLET in 1 BLISTER PACK (70518-0579-7)Marketed from Feb 11, 2023

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
REMEDYREPACK INC.NDC labeler code 70518
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 70518-0579_5c17d78a-468d-dad7-e063-6294a90aa453SPL ID 5c17d78a-468d-dad7-e063-6294a90aa453
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

N470518057900 followed by a unit qualifier and the quantity

Package 70518-0579-00. 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 70518-0579

What is NDC 70518-0579?
70518-0579 is the product NDC for Glipizide, Glipizide 10 mg/1 tablet, listed with the FDA by REMEDYREPACK 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?
REMEDYREPACK INC., NDC labeler code 70518. 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/1TabletOralAvPAK50268-361
GlipizideGlipizide 10 mg/1TabletOralAvPAK50268-362
GlipizideGlipizide 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-130
GlipizideGlipizide 5 mg/1TabletOralREMEDYREPACK INC.70518-0552
GlipizideGlipizide 10 mg/1TabletOralProficient Rx LP63187-993
GlipizideGlipizide 5 mg/1TabletOralCoupler LLC67046-0236
GlipizideGlipizide 5 mg/1TabletOralCardinal Health 107, LLC55154-7987
GlipizideGlipizide 10 mg/1TabletOralCoupler LLC67046-0367
GlipizideGlipizide 5 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-0141
GlipizideGlipizide 10 mg/1TabletOralBryant Ranch Prepack72162-2102
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack72162-2103
GlipizideGlipizide 10 mg/1TabletOralA-S Medication Solutions50090-7197
GlipizideGlipizide 10 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-0142
GlipizideGlipizide 10 mg/1TabletOralNorthwind Health Company, LLC51655-106
GlipizideGlipizide 5 mg/1TabletOralLegacy Pharmaceutical Packaging, LLC68645-574
GlipizideGlipizide 10 mg/1TabletOralLegacy Pharmaceutical Packaging, LLC68645-575
GlipizideGlipizide 5 mg/1TabletOralBryant Ranch Prepack71335-0930
GlipizideGlipizide 5 mg/1TabletOralNorthwind Health Company, LLC51655-180
GlipizideGlipizide 5 mg/1TabletOralProficient Rx LP71205-041
GlipizideGlipizide 5 mg/1TabletOralAmerican Health Packaging60687-690

Showing 20 of 35.

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