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NDC 69880-120, Octreotide, capsule, delayed release, from Amryt Pharmaceuticals Designated Activity Company.

Product NDC
69880-120
Status
Listed
Labeler
Amryt Pharmaceuticals Designated Activity Company
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA208232
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69880-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OCTREOTIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69880-120-28698800120284 BLISTER PACK in 1 DOSE PACK (69880-120-28) / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/62a5e1eb-b48e-4ea6-8781-f75e490b17e4

Use it

Look up 69880-120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69880-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69880-120. 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.