NDC codes

FDA NDC Directory
Product NDC (as listed)62135-732Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62135-0732Add 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
62135-732-606213507326060 TABLET, FILM COATED in 1 BOTTLE (62135-732-60)Marketed from Aug 15, 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 and metformin hcl
Generic name (nonproprietary)
glipizide and metformin hcl
Active ingredients
Glipizide — 2.5 mg/1Metformin hydrochloride — 500 mg/1
Dosage form
Tablet, Film coated
Route
Oral
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 62135-732_459bebab-b18b-58b4-e063-6294a90ad140SPL ID 459bebab-b18b-58b4-e063-6294a90ad140SPL set ID ac018f64-fd9d-4b3c-b0ac-ca305b8df635RxCUI 861731, 861736, 861740UNII 786Z46389E, X7WDT95N5CUPC 0362135733605, 0362135731601, 0362135732608
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

N462135073260 followed by a unit qualifier and the quantity

Package 62135-0732-60. 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 . This label includes a boxed warning.

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)

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 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralChartwell RX, LLC62135-733
Glipizide and Metformin HClGlipizide 5 mg/1; Metformin hydrochloride 500 mg/1Tablet, Film coatedOralProficient Rx LP71205-270

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