Prescription drug · NDA
Lorbrena (Lorlatinib) NDC 0069-0231
Lorlatinib 100 mg/1 · Tablet, Film coated · Oral · Pfizer Laboratories Div Pfizer Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0069-0231-01 | 00069023101 | 30 TABLET, FILM COATED in 1 BOTTLE (0069-0231-01)Marketed from Nov 19, 2018 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
- Lorbrena
- Generic name (nonproprietary)
- lorlatinib
- Active ingredients
- Lorlatinib — 100 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Pfizer Laboratories Div Pfizer IncNDC labeler code 0069
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 210868
- Marketing start
- Listing expires
- Other FDA classes
- Breast Cancer Resistance Protein Inhibitors (Mechanism)Cytochrome P450 2B6 Inducers (Mechanism)Cytochrome P450 3A Inducers (Mechanism)Kinase Inhibitors (Mechanism)Multidrug and Toxin Extrusion Transporter 1 Inhibitors (Mechanism)Organic Anion Transporter 3 Inhibitors (Mechanism)Organic Cation Transporter 1 Inhibitors (Mechanism)P-Glycoprotein Inducers (Mechanism)
- Identifiers
- Product ID 0069-0231_46cb56ce-da15-49af-b72b-f9e377cae4a6SPL ID 46cb56ce-da15-49af-b72b-f9e377cae4a6SPL set ID 2b34d62d-e02a-4af3-bc0d-1571dd4ee76dRxCUI 2103169, 2103175, 2103177, 2103179UNII OSP71S83EUUPC 0300690231013, 0300690227016
- Pharmacologic class
- Kinase Inhibitor
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
N400069023101followed by a unit qualifier and the quantityPackage 00069-0231-01. 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
Current FDA label (SPL), effective .
Indications (excerpt from the label)
LORBRENA ® is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK)-positive as detected by an FDA-approved test. LORBRENA is a kinase inhibitor indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors are anaplastic lymphoma kinase (ALK)-positive as detected by an FDA-approved test. ( 1 , 2.1 )
Excerpt only. Read the full label for complete information.
About NDC 0069-0231
- What is NDC 0069-0231?
- 0069-0231 is the product NDC for Lorbrena (lorlatinib), Lorlatinib 100 mg/1 tablet, film coated, listed with the FDA by Pfizer Laboratories Div Pfizer Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Lorbrena (Lorlatinib).
- What is the active ingredient?
- Lorlatinib.
- Who is the labeler?
- Pfizer Laboratories Div Pfizer Inc, NDC labeler code 0069. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Lorbrena?
- 2 other product NDCs are listed under this name. See all Lorbrena NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Lorbrena products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Lorbrenalorlatinib | Lorlatinib 25 mg/1 | Tablet, Film coatedOral | U.S. Pharmaceuticals | 63539-927 | 63539-0927-01 |
| Lorbrenalorlatinib | Lorlatinib 25 mg/1 | Tablet, Film coatedOral | Pfizer Laboratories Div Pfizer Inc | 0069-0227 | 00069-0227-0100069-0227-03 |
Other NDCs under NDA 210868
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 |
|---|---|---|---|---|
| Lorbrenalorlatinib | Lorlatinib 25 mg/1 | Tablet, Film coatedOral | Pfizer Laboratories Div Pfizer Inc | 0069-0227 |
| Lorbrenalorlatinib | Lorlatinib 25 mg/1 | Tablet, Film coatedOral | U.S. Pharmaceuticals | 63539-927 |