herceptin
Generic: trastuzumab
Labeler: genentech, inc.Drug Facts
Product Profile
Brand Name
herceptin
Generic Name
trastuzumab
Labeler
genentech, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
trastuzumab 150 mg/7.4mL
Manufacturer
Identifiers & Regulatory
Product NDC
50242-132
Product ID
50242-132_5e75840c-4462-440a-9e17-caa80dd4127b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA103792
Listing Expiration
2026-12-31
Marketing Start
2017-02-10
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50242132
Hyphenated Format
50242-132
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
herceptin (source: ndc)
Generic Name
trastuzumab (source: ndc)
Application Number
BLA103792 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/7.4mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (50242-132-01) / 15 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5e75840c-4462-440a-9e17-caa80dd4127b", "openfda": {"nui": ["N0000175661", "N0000020008"], "unii": ["P188ANX8CK"], "rxcui": ["1922509", "1922512"], "spl_set_id": ["492dbdb2-077e-4064-bff3-372d6af0a7a2"], "pharm_class_epc": ["HER2/neu Receptor Antagonist [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 (50242-132-01) / 15 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "50242-132-01", "marketing_start_date": "20170210"}], "brand_name": "Herceptin", "product_id": "50242-132_5e75840c-4462-440a-9e17-caa80dd4127b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["HER2/Neu/cerbB2 Antagonists [MoA]", "HER2/neu Receptor Antagonist [EPC]"], "product_ndc": "50242-132", "generic_name": "Trastuzumab", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Herceptin", "active_ingredients": [{"name": "TRASTUZUMAB", "strength": "150 mg/7.4mL"}], "application_number": "BLA103792", "marketing_category": "BLA", "marketing_start_date": "20170210", "listing_expiration_date": "20261231"}