United States · FDA National Drug Code directory
Octreotide
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
- 63323-377_d8819119-418c-494a-8ab5-d9502c7aed93
- Product NDC
- 63323-377
- Form
- INJECTION, SOLUTION
- Composition / generic term
- OCTREOTIDE ACETATE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060314
- Source listing expiry
- 20261231
Source-listed ingredients
- OCTREOTIDE ACETATE — 500 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-377-04) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-377-41) · 63323-377-04
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 →