63323-379 : Octreotide 1000 ug/ml Intravenous; Subcutaneous Injection, Solution


NDC: 63323-379
Labeler: Fresenius Kabi USA, LLC
Product Type: Human Prescription Drug
Drug Name:  Octreotide
Dosage Form: Intravenous; Subcutaneous Injection, Solution
Application #: ANDA077450
Rev. Date: 


NDC Package Codes:

  • 63323-379-05: 1 VIAL, MULTI‑DOSE IN 1 CARTON (63323‑379‑05) > 5 ML IN 1 VIAL, MULTI‑DOSE

Active Ingredients:

  • Octreotide Acetate

Dosage Strength:

  • 1000 ug/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 63323-365 Octreotide 50 ug/ml Intravenous; Subcutaneous Injection, Solution by Fresenius Kabi USA, LLC
  • 63323-376 Octreotide 100 ug/ml Intravenous; Subcutaneous Injection, Solution by Fresenius Kabi USA, LLC
  • 63323-377 Octreotide 500 ug/ml Intravenous; Subcutaneous Injection, Solution by Fresenius Kabi USA, LLC
  • 63323-378 Octreotide 200 ug/ml Intravenous; Subcutaneous Injection, Solution by Fresenius Kabi USA, LLC

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.