Prescription drug · ANDA
Glipizide NDC 70518-2308
Glipizide 2.5 mg/1 · Tablet, Film coated, Extended release · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-2308-0 | 70518230800 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2308-0)Marketed from Sep 11, 2019 | |
| 70518-2308-1 | 70518230801 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2308-1)Marketed from Aug 27, 2025 |
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 — 2.5 mg/1
- Dosage form
- Tablet, Film coated, Extended release
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 204720
- Marketing start
- Listing expires
- Other FDA classes
- Sulfonylurea Compounds (Chemical structure)
- Identifiers
- Product ID 70518-2308_4a007068-89db-c296-e063-6394a90ad6d0SPL ID 4a007068-89db-c296-e063-6394a90ad6d0SPL set ID bde478e6-e290-47e0-9241-ce88d927633eRxCUI 310489UNII X7WDT95N5C
- 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
N470518230800followed by a unit qualifier and the quantityPackage 70518-2308-00. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 204720
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Glipizide | Glipizide 10 mg/1 | Tablet, Film coated, Extended releaseOral | REMEDYREPACK INC. | 70518-1848 |
| Glipizide | Glipizide 10 mg/1 | Tablet, Film coated, Extended releaseOral | Preferred Pharmaceuticals Inc. | 68788-7856 |
| Glipizide | Glipizide 10 mg/1 | Tablet, Film coated, Extended releaseOral | A-S Medication Solutions | 50090-5806 |
| Glipizide | Glipizide 10 mg/1 | Tablet, Film coated, Extended releaseOral | Northwind Health Company, LLC | 51655-966 |
| Glipizide | Glipizide 2.5 mg/1 | Tablet, Film coated, Extended releaseOral | Preferred Pharmaceuticals Inc. | 68788-8487 |
| Glipizide | Glipizide 5 mg/1 | Tablet, Film coated, Extended releaseOral | Bryant Ranch Prepack | 71335-1031 |
| Glipizide | Glipizide 2.5 mg/1 | Tablet, Film coated, Extended releaseOral | Bryant Ranch Prepack | 71335-1042 |
| Glipizide | Glipizide 5 mg/1 | Tablet, Film coated, Extended releaseOral | REMEDYREPACK INC. | 70518-1063 |
| Glipizide | Glipizide 10 mg/1 | Tablet, Film coated, Extended releaseOral | Bryant Ranch Prepack | 71335-1130 |
| Glipizide | Glipizide 2.5 mg/1 | Tablet, Film coated, Extended releaseOral | Rising Pharma Holdings, Inc. | 64980-279 |
| Glipizide | Glipizide 5 mg/1 | Tablet, Film coated, Extended releaseOral | Rising Pharma Holdings, Inc. | 64980-280 |
| Glipizide | Glipizide 10 mg/1 | Tablet, Film coated, Extended releaseOral | Rising Pharma Holdings, Inc. | 64980-281 |
| Glipizide | Glipizide 5 mg/1 | Tablet, Film coated, Extended releaseOral | Northwind Health Company, LLC | 51655-337 |
| Glipizide | Glipizide 5 mg/1 | Tablet, Film coated, Extended releaseOral | A-S Medication Solutions | 50090-5040 |