vivimusta

Generic: bendamustine hydrochloride

Labeler: azurity pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name vivimusta
Generic Name bendamustine hydrochloride
Labeler azurity pharmaceuticals, inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

bendamustine hydrochloride 25 mg/mL

Manufacturer
Azurity Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 24338-270
Product ID 24338-270_24f87fb8-dc5d-4daf-8afc-047afe1bcfee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA212209
Listing Expiration 2026-12-31
Marketing Start 2025-04-01

Pharmacologic Class

Classes
alkylating activity [moa] alkylating drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24338270
Hyphenated Format 24338-270

Supplemental Identifiers

RxCUI
1726097 2622914
UNII
981Y8SX18M

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 vivimusta (source: ndc)
Generic Name bendamustine hydrochloride (source: ndc)
Application Number NDA212209 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (24338-270-01) / 4 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

24338-270-01 1 VIAL, MULTI-DOSE in 1 CARTON (24338-270-01) / 4 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

bendamustine hydrochloride (25 mg/mL)

Linked Drug Pages (1)

VIVIMUSTA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "24f87fb8-dc5d-4daf-8afc-047afe1bcfee", "openfda": {"unii": ["981Y8SX18M"], "rxcui": ["1726097", "2622914"], "spl_set_id": ["4df6548f-c4ad-4eb2-a54f-19766a3d90ca"], "manufacturer_name": ["Azurity Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (24338-270-01)  / 4 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "24338-270-01", "marketing_start_date": "20250401"}], "brand_name": "VIVIMUSTA", "product_id": "24338-270_24f87fb8-dc5d-4daf-8afc-047afe1bcfee", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "24338-270", "generic_name": "BENDAMUSTINE HYDROCHLORIDE", "labeler_name": "Azurity Pharmaceuticals, Inc.", "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": "20250401", "listing_expiration_date": "20261231"}