Lorbrena is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Pfizer Laboratories Div Pfizer Inc. The primary component is Lorlatinib.
| Product ID | 0069-0231_4b051995-d812-4f93-87a1-6f53431bf7dc |
| NDC | 0069-0231 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lorbrena |
| Generic Name | Lorlatinib |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2018-11-19 |
| Marketing Category | NDA / NDA |
| Application Number | NDA210868 |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | LORLATINIB |
| Active Ingredient Strength | 100 mg/1 |
| Pharm Classes | Kinase Inhibitor [EPC],Kinase Inhibitors [MoA],Cytochrome P450 3A4 Inducers [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2018-11-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA210868 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2018-11-19 |
| Ingredient | Strength |
|---|---|
| LORLATINIB | 100 mg/1 |
| SPL SET ID: | 2b34d62d-e02a-4af3-bc0d-1571dd4ee76d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0069-0227 | Lorbrena | lorlatinib |
| 0069-0231 | Lorbrena | lorlatinib |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LORBRENA 86821577 5396892 Live/Registered |
Pfizer Inc. 2015-11-16 |