herceptin

Generic: trastuzumab

Labeler: genentech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name herceptin
Generic Name trastuzumab
Labeler genentech, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

trastuzumab 150 mg/7.4mL

Manufacturer
Genentech, Inc.

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)
her2/neu receptor antagonist [epc]
Mechanism of Action
her2/neu/cerbb2 antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50242132
Hyphenated Format 50242-132

Supplemental Identifiers

RxCUI
1922509 1922512
UNII
P188ANX8CK
NUI
N0000175661 N0000020008

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 150 mg/7.4mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (50242-132-01) / 15 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

trastuzumab (150 mg/7.4mL)

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"}