Prescription drug · ANDA
Lurasidone Hydrochloride NDC 65162-879
Lurasidone hydrochloride 20 mg/1 · Tablet, Coated · Oral · Amneal Pharmaceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 65162-879-03 | 65162087903 | 30 TABLET, COATED in 1 BOTTLE (65162-879-03)Marketed from Jan 2, 2023 | |
| 65162-879-09 | 65162087909 | 90 TABLET, COATED in 1 BOTTLE (65162-879-09)Marketed from Jan 2, 2023 | |
| 65162-879-50 | 65162087950 | 500 TABLET, COATED in 1 BOTTLE (65162-879-50)Marketed from Jan 2, 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 — 20 mg/1
- Dosage form
- Tablet, Coated
- Route
- Oral
- Labeler
- Amneal Pharmaceuticals LLCNDC labeler code 65162
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 208002
- Marketing start
- Listing expires
- Identifiers
- Product ID 65162-879_cfb63983-dd01-4006-b387-7e8cfec0699dSPL ID cfb63983-dd01-4006-b387-7e8cfec0699dSPL set ID 6ef0b2f9-9356-4f61-a2fa-e7c2c77a5d3aRxCUI 1040031, 1040041, 1235247, 1297278, 1431235UNII O0P4I5851IUPC 0365162882032, 0365162880038, 0365162879032, 0365162082036, 0365162881035
- 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
N465162087903followed by a unit qualifier and the quantityPackage 65162-0879-03. 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: 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: Depressive episode associated with Bipolar I Disorder (bipolar depression) in adults and pediatric patients (10 to 17 years) as monotherapy. ( 1 , 14.2 ) Depressive episode associated with…
Excerpt only. Read the full label for complete information.
About NDC 65162-879
- What is NDC 65162-879?
- 65162-879 is the product NDC for Lurasidone Hydrochloride, Lurasidone hydrochloride 20 mg/1 tablet, coated, listed with the FDA by Amneal Pharmaceuticals LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Lurasidone Hydrochloride.
- What is the active ingredient?
- Lurasidone hydrochloride.
- Who is the labeler?
- Amneal Pharmaceuticals LLC, NDC labeler code 65162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Lurasidone Hydrochloride?
- 127 other product NDCs are listed under this name. See all Lurasidone Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Lurasidone Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Lurasidone Hydrochloride | Lurasidone hydrochloride 60 mg/1 | Tablet, Film coatedOral | Torrent Pharmaceuticals Limited | 13668-737 | 13668-0737-3013668-0737-90 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 60 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1659 | 67046-1659-03 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 20 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4563 | 70518-4563-00 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 60 mg/1 | TabletOral | Coupler LLC | 67046-1654 | 67046-1654-03 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 40 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1637 | 67046-1637-03 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 40 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4491 | 70518-4491-00 |
| lurasidone hydrochloride | Lurasidone hydrochloride 40 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4427 | 70518-4427-00 |
| lurasidone hydrochloride | Lurasidone hydrochloride 20 mg/1 | Tablet, Film coatedOral | NorthStar RxLLC | 72603-621 | 72603-0621-01 |
| lurasidone hydrochloride | Lurasidone hydrochloride 40 mg/1 | Tablet, Film coatedOral | NorthStar RxLLC | 72603-622 | 72603-0622-01 |
| lurasidone hydrochloride | Lurasidone hydrochloride 60 mg/1 | Tablet, Film coatedOral | NorthStar RxLLC | 72603-623 | 72603-0623-01 |
Other NDCs under ANDA 208002
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 60 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals of New York LLC | 53746-082 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 20 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals of New York LLC | 53746-879 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 40 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals of New York LLC | 53746-880 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 80 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals of New York LLC | 53746-881 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 120 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals of New York LLC | 53746-882 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 60 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals LLC | 65162-082 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 40 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals LLC | 65162-880 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 80 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals LLC | 65162-881 |
| Lurasidone Hydrochloride | Lurasidone hydrochloride 120 mg/1 | Tablet, CoatedOral | Amneal Pharmaceuticals LLC | 65162-882 |