United States · FDA National Drug Code directory
OCTREOTIDE ACETATE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 23155-685_b90ce9b0-5886-4b4f-a721-9698fa28a7ec
- Product NDC
- 23155-685
- Form
- INJECTION, SOLUTION
- Composition / generic term
- octreotide acetate
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220525
- Source listing expiry
- 20261231
Source-listed ingredients
- OCTREOTIDE ACETATE — 200 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 mL in 1 VIAL, GLASS (23155-685-31) · 23155-685-31
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →