Prescription drug · ANDA
lurasidone hydrochloride NDC 68180-672
Lurasidone hydrochloride 60 mg/1 · Tablet · Oral · Lupin Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68180-672-06 | 68180067206 | 30 TABLET in 1 BOTTLE (68180-672-06)Marketed from Feb 20, 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)
- lurasidone hydrochloride
- Generic name (nonproprietary)
- lurasidone hydrochloride
- Active ingredients
- Lurasidone hydrochloride — 60 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Lupin Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208031
- Marketing start
- Listing expires
- Identifiers
- Product ID 68180-672_8d77b0dd-8cc2-44da-afed-1e5cb75bed99SPL ID 8d77b0dd-8cc2-44da-afed-1e5cb75bed99SPL set ID 74f2429b-71df-47f0-9cb5-98685372a9b8RxCUI 1040031, 1040041, 1235247, 1297278, 1431235UNII O0P4I5851IUPC 0368180671060, 0368180673064, 0368180672067, 0368180670063, 0368180674061
- Pharmacologic class
- Atypical 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
N468180067206followed by a unit qualifier and the quantityPackage 68180-0672-06. 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)
Lurasidone hydrochloride tablets are indicated for: Treatment of adult and adolescent patients (13 to 17 years) with schizophrenia [see Clinical Studies ( 14.1 )] . Monotherapy treatment of adult and pediatric patients (10 to 17 years) with major depressive episode associated with bipolar I disorder (bipolar depression) [see Clinical Studies ( 14.2 )] . Adjunctive treatment with lithium or valproate in adult patients with major depressive episode associated with bipolar I disorder (bipolar depression) [see Clinical Studies ( 14.2 )] . Lurasidone hydrochloride is an atypical antipsychotic indicated for the treatment of: Schizophrenia in adults and adolescents (13 to 17 years) ( 1 , 14.1 ) Dep…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 208031
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 |
|---|---|---|---|---|
| lurasidone hydrochloride | Lurasidone hydrochloride 40 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-671 |
| lurasidone hydrochloride | Lurasidone hydrochloride 20 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-670 |
| lurasidone hydrochloride | Lurasidone hydrochloride 80 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-673 |
| lurasidone hydrochloride | Lurasidone hydrochloride 120 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-674 |
| lurasidone hydrochloride | Lurasidone hydrochloride 40 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4427 |