0078-0184 : Sandostatin 1000 ug/ml Intravenous; Subcutaneous Injection, Solution
| NDC: | 0078-0184 |
| Labeler: | Novartis Pharmaceuticals Corporation |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Sandostatin |
| Dosage Form: | Intravenous; Subcutaneous Injection, Solution |
| Application #: | NDA019667 |
| Rev. Date: |
NDC Package Codes:
- 0078-0184-25: 1 VIAL, MULTI‑DOSE IN 1 BOX (0078‑0184‑25) > 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.- 0078-0180 Sandostatin 50 ug/ml Intravenous; Subcutaneous Injection, Solution by Novartis Pharmaceuticals Corporation
- 0078-0181 Sandostatin 100 ug/ml Intravenous; Subcutaneous Injection, Solution by Novartis Pharmaceuticals Corporation
- 0078-0182 Sandostatin 500 ug/ml Intravenous; Subcutaneous Injection, Solution by Novartis Pharmaceuticals Corporation
- 0078-0183 Sandostatin 200 ug/ml Intravenous; Subcutaneous Injection, Solution by Novartis Pharmaceuticals Corporation
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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.