vivimusta
Generic: bendamustine hydrochloride
Labeler: slayback pharma llcDrug Facts
Product Profile
Brand Name
vivimusta
Generic Name
bendamustine hydrochloride
Labeler
slayback pharma llc
Dosage Form
INJECTION
Routes
Active Ingredients
bendamustine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71225-120
Product ID
71225-120_c4b54079-dac2-4e01-a00f-6ceaa788f605
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA212209
Listing Expiration
2026-12-31
Marketing Start
2022-12-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71225120
Hyphenated Format
71225-120
Supplemental Identifiers
RxCUI
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
vivimusta (source: ndc)
Generic Name
bendamustine hydrochloride (source: ndc)
Application Number
NDA212209 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (71225-120-01) / 4 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c4b54079-dac2-4e01-a00f-6ceaa788f605", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1726097", "2622914"], "spl_set_id": ["cbcc6eb7-aa62-4599-af49-05203fedb4bb"], "manufacturer_name": ["Slayback Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71225-120-01) / 4 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71225-120-01", "marketing_start_date": "20221207"}], "brand_name": "VIVIMUSTA", "product_id": "71225-120_c4b54079-dac2-4e01-a00f-6ceaa788f605", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "71225-120", "generic_name": "BENDAMUSTINE HYDROCHLORIDE", "labeler_name": "Slayback Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VIVIMUSTA", "active_ingredients": [{"name": "BENDAMUSTINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "NDA212209", "marketing_category": "NDA", "marketing_start_date": "20221207", "listing_expiration_date": "20261231"}