lumakras
Generic: sotorasib
Labeler: amgen incDrug Facts
Product Profile
Brand Name
lumakras
Generic Name
sotorasib
Labeler
amgen inc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
sotorasib 240 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55513-512
Product ID
55513-512_8f611e67-8c58-4413-8b81-a200fa7f30e8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA214665
Listing Expiration
2026-12-31
Marketing Start
2024-06-27
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55513512
Hyphenated Format
55513-512
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lumakras (source: ndc)
Generic Name
sotorasib (source: ndc)
Application Number
NDA214665 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 240 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (55513-512-60) / 120 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f611e67-8c58-4413-8b81-a200fa7f30e8", "openfda": {"upc": ["0355513488020", "0000000000000", "0355513488242", "0355513504508"], "unii": ["2B2VM6UC8G"], "rxcui": ["2550719", "2550725", "2628240", "2628242", "2687205", "2687207"], "spl_set_id": ["c80a362c-7ac3-4894-a076-0691e68ef8c1"], "manufacturer_name": ["Amgen Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (55513-512-60) / 120 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "55513-512-60", "marketing_start_date": "20240627"}], "brand_name": "LUMAKRAS", "product_id": "55513-512_8f611e67-8c58-4413-8b81-a200fa7f30e8", "dosage_form": "TABLET, COATED", "product_ndc": "55513-512", "generic_name": "sotorasib", "labeler_name": "Amgen Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LUMAKRAS", "active_ingredients": [{"name": "SOTORASIB", "strength": "240 mg/1"}], "application_number": "NDA214665", "marketing_category": "NDA", "marketing_start_date": "20240627", "listing_expiration_date": "20261231"}