NDC codes

FDA NDC Directory
Product NDC (as listed)71205-270Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0270Add 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
71205-270-30712050270307120502703030 TABLET, FILM COATED in 1 BOTTLE (71205-270-30)Marketed from May 1, 2019
71205-270-60712050270607120502706060 TABLET, FILM COATED in 1 BOTTLE (71205-270-60)Marketed from May 1, 2019
71205-270-90712050270907120502709090 TABLET, FILM COATED in 1 BOTTLE (71205-270-90)Marketed from May 1, 2019

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 and Metformin HCl
Generic name (nonproprietary)
glipizide and metformin hcl
Active ingredients
Glipizide — 5 mg/1Metformin hydrochloride — 500 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078728
Marketing start
Listing expires
Other FDA classes
Biguanides (Chemical structure)Sulfonylurea Compounds (Chemical structure)
Identifiers
Product ID 71205-270_ba23a55b-30dd-4d55-a423-3542524a8efeSPL ID ba23a55b-30dd-4d55-a423-3542524a8efeSPL set ID be4d2552-c964-4d09-ba7a-0d94320f968cRxCUI 861740UNII X7WDT95N5C, 786Z46389E
Pharmacologic class
Biguanide; 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

N471205027030 followed by a unit qualifier and the quantity

Package 71205-0270-30. 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 and Metformin HCl 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 71205-270

What is NDC 71205-270?
71205-270 is the product NDC for Glipizide and Metformin HCl, Glipizide 5 mg/1; Metformin hydrochloride 500 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Glipizide and Metformin HCl.
What is the active ingredient?
Glipizide, Metformin hydrochloride.
Who is the labeler?
Proficient Rx LP, NDC labeler code 71205. 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 and Metformin HCl?
6 other product NDCs are listed under this name. See all Glipizide and Metformin HCl 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 and Metformin HCl NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Glipizide and Metformin HClGlipizide 2.5 mg/1; Metformin hydrochloride 250 mg/1Tablet, Film coatedOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-11523155-0115-0123155-0115-10
Glipizide and Metformin HClGlipizide 2.5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-11623155-0116-0123155-0116-10
Glipizide and Metformin HClGlipizide 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-11723155-0117-0123155-0117-10
Glipizide and metformin hclGlipizide 2.5 mg/1; Metformin hydrochloride 250 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-73162135-0731-60
Glipizide and metformin hclGlipizide 2.5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-73262135-0732-60
Glipizide and metformin hclGlipizide 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-73362135-0733-60

Other NDCs under ANDA 078728

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

FDA NDC Directory listings under ANDA 078728
ProductStrengthForm · routeLabelerProduct NDC
Glipizide and Metformin HClGlipizide 2.5 mg/1; Metformin hydrochloride 250 mg/1Tablet, Film coatedOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-115
Glipizide and Metformin HClGlipizide 2.5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-116
Glipizide and Metformin HClGlipizide 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-117
Glipizide and metformin hclGlipizide 2.5 mg/1; Metformin hydrochloride 250 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-731
Glipizide and metformin hclGlipizide 2.5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-732
Glipizide and metformin hclGlipizide 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-733

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