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bendamustine hydrochloride

NDC 68001-572, bendamustine hydrochloride, injection, powder, lyophilized, for solution, from BluePoint Laboratories.

Product NDC
68001-572
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205574
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-572 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENDAMUSTINE HYDROCHLORIDE100 mg/20mL

Pharmacologic classes

Alkylating Activity [MoA]; Alkylating Drug [EPC]

Package NDCNDC-11Package
68001-572-41680010572411 VIAL, SINGLE-DOSE in 1 CARTON (68001-572-41) / 20 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0df025d2-c093-427a-b599-f605e71fe835

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68001-572

Use it

Look up 68001-572 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-572 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-572. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.