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gemcitabine

NDC 55111-687, gemcitabine, injection, powder, lyophilized, for solution, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-687
Status
Listed
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091365
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-687 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GEMCITABINE HYDROCHLORIDE1 g/25mL

Pharmacologic classes

Nucleic Acid Synthesis Inhibitors [MoA]; Nucleoside Metabolic Inhibitor [EPC]

Package NDCNDC-11Package
55111-687-25551110687251 VIAL, SINGLE-USE in 1 CARTON (55111-687-25) / 25 mL in 1 VIAL, SINGLE-USE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eafcebc8-ddef-bb6b-fd0a-9d8b9962cdc4

Use it

Look up 55111-687 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-687 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-687. 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.