Prescription drug · ANDA
Repaglinide NDC 65862-672
Repaglinide 2 mg/1 · Tablet · Oral · Aurobindo Pharma Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 65862-672-01 | 65862067201 | 100 TABLET in 1 BOTTLE (65862-672-01)Marketed from Jan 22, 2014 | |
| 65862-672-05 | 65862067205 | 500 TABLET in 1 BOTTLE (65862-672-05)Marketed from Jan 22, 2014 | |
| 65862-672-99 | 65862067299 | 1000 TABLET in 1 BOTTLE (65862-672-99)Marketed from Jan 22, 2014 |
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)
- Repaglinide
- Generic name (nonproprietary)
- repaglinide
- Active ingredients
- Repaglinide — 2 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Aurobindo Pharma Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 203820
- Marketing start
- Listing expires
- Other FDA classes
- Potassium Channel Antagonists (Mechanism)
- Identifiers
- Product ID 65862-672_54d938ac-ebf2-49d0-8056-f65d8aadfb98SPL ID 54d938ac-ebf2-49d0-8056-f65d8aadfb98SPL set ID 68064989-47ea-4ed5-a20e-43c4ef6ec271RxCUI 200256, 200257, 200258UNII 668Z8C33LUUPC 0365862670014, 0365862672018, 0365862671011
- Pharmacologic class
- Glinide
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
N465862067201followed by a unit qualifier and the quantityPackage 65862-0672-01. 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 203820
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 |
|---|---|---|---|---|
| Repaglinide | Repaglinide 1 mg/1 | TabletOral | American Health Packaging | 60687-560 |
| Repaglinide | Repaglinide .5 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-670 |
| Repaglinide | Repaglinide 1 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-671 |
| Repaglinide | Repaglinide .5 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-4866 |
| Repaglinide | Repaglinide 1 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-2558 |
| Repaglinide | Repaglinide 2 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-159 |
| Repaglinide | Repaglinide .5 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-157 |
| Repaglinide | Repaglinide 1 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-158 |