Prescription drug · ANDA
Haloperidol NDC 59651-793
Haloperidol 10 mg/1 · Tablet · Oral · Aurobindo Pharma Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59651-793-01 | 59651079301 | 100 TABLET in 1 BOTTLE (59651-793-01)Marketed from Apr 19, 2024 | |
| 59651-793-99 | 59651079399 | 1000 TABLET in 1 BOTTLE (59651-793-99)Marketed from Apr 19, 2024 |
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)
- Haloperidol
- Generic name (nonproprietary)
- haloperidol
- Active ingredients
- Haloperidol — 10 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 218789
- Marketing start
- Listing expires
- Identifiers
- Product ID 59651-793_265a70c4-9b29-464c-9258-735bd2b2ccf7SPL ID 265a70c4-9b29-464c-9258-735bd2b2ccf7SPL set ID bf21633e-f37b-4017-a143-538eb005de2dRxCUI 197754, 310670, 310671, 310672, 314034, 314035UNII J6292F8L3D
- Pharmacologic class
- Typical Antipsychotic
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
N459651079301followed by a unit qualifier and the quantityPackage 59651-0793-01. 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 218789
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 |
|---|---|---|---|---|
| Haloperidol | Haloperidol 20 mg/1 | TabletOral | Coupler LLC | 67046-1673 |
| Haloperidol | Haloperidol .5 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-789 |
| Haloperidol | Haloperidol 2 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-791 |
| Haloperidol | Haloperidol 1 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-790 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-792 |
| Haloperidol | Haloperidol 20 mg/1 | TabletOral | Aurobindo Pharma Limited | 59651-794 |
| Haloperidol | Haloperidol 2 mg/1 | TabletOral | Coupler LLC | 67046-1498 |
| Haloperidol | Haloperidol 1 mg/1 | TabletOral | Coupler LLC | 67046-1548 |
| Haloperidol | Haloperidol 2 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2937 |
| Haloperidol | Haloperidol 5 mg/1 | TabletOral | Coupler LLC | 67046-1603 |