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Octreotide Acetate

NDC 71288-567, Octreotide Acetate, injection, solution, from Meitheal Pharmaceuticals, Inc..

Product NDC
71288-567
Status
Listed
Labeler
Meitheal Pharmaceuticals, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71288-567 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OCTREOTIDE ACETATE100 ug/mL

Pharmacologic classes

Somatostatin Analog [EPC]; Somatostatin Receptor Agonists [MoA]

Package NDCNDC-11Package
71288-567-027128805670210 VIAL, SINGLE-DOSE in 1 CARTON (71288-567-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-567-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/01962c67-e551-47b6-a276-e1ae1860d2a4

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=71288-567

Use it

Look up 71288-567 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71288-567 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71288-567. 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.