phesgo
Generic: pertuzumab, trastuzumab, and hyaluronidase-zzxf
Labeler: genentech, inc.Drug Facts
Product Profile
Brand Name
phesgo
Generic Name
pertuzumab, trastuzumab, and hyaluronidase-zzxf
Labeler
genentech, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
hyaluronidase (human recombinant) 30000 U/15mL, pertuzumab 1200 mg/15mL, trastuzumab 600 mg/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
50242-245
Product ID
50242-245_c871709f-bb8a-4e51-91ad-31c75d43548e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA761170
Listing Expiration
2026-12-31
Marketing Start
2020-06-29
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50242245
Hyphenated Format
50242-245
Supplemental Identifiers
RxCUI
UNII
NUI
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
phesgo (source: ndc)
Generic Name
pertuzumab, trastuzumab, and hyaluronidase-zzxf (source: ndc)
Application Number
BLA761170 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30000 U/15mL
- 1200 mg/15mL
- 600 mg/15mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (50242-245-01) / 15 mL in 1 VIAL, SINGLE-DOSE
- 1 VIAL, SINGLE-DOSE in 1 CARTON (50242-245-86) / 15 mL in 1 VIAL, SINGLE-DOSE
Packages (2)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "c871709f-bb8a-4e51-91ad-31c75d43548e", "openfda": {"nui": ["N0000175661", "N0000020008", "N0000175531", "M0009499"], "unii": ["P188ANX8CK", "K16AIQ8CTM", "743QUY4VD8"], "rxcui": ["2382604", "2382609", "2383305", "2383307"], "spl_set_id": ["27dd5e6b-72cd-458d-a015-cf4dab5800da"], "pharm_class_cs": ["Glycoside Hydrolases [CS]"], "pharm_class_epc": ["HER2/neu Receptor Antagonist [EPC]", "Endoglycosidase [EPC]"], "pharm_class_moa": ["HER2/Neu/cerbB2 Antagonists [MoA]"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (50242-245-01) / 15 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50242-245-01", "marketing_start_date": "20200629"}, {"sample": true, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (50242-245-86) / 15 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50242-245-86", "marketing_start_date": "20210503"}], "brand_name": "Phesgo", "product_id": "50242-245_c871709f-bb8a-4e51-91ad-31c75d43548e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Endoglycosidase [EPC]", "Glycoside Hydrolases [CS]", "HER2/Neu/cerbB2 Antagonists [MoA]", "HER2/Neu/cerbB2 Antagonists [MoA]", "HER2/neu Receptor Antagonist [EPC]", "HER2/neu Receptor Antagonist [EPC]"], "product_ndc": "50242-245", "generic_name": "pertuzumab, trastuzumab, and hyaluronidase-zzxf", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phesgo", "active_ingredients": [{"name": "HYALURONIDASE (HUMAN RECOMBINANT)", "strength": "30000 U/15mL"}, {"name": "PERTUZUMAB", "strength": "1200 mg/15mL"}, {"name": "TRASTUZUMAB", "strength": "600 mg/15mL"}], "application_number": "BLA761170", "marketing_category": "BLA", "marketing_start_date": "20200629", "listing_expiration_date": "20261231"}