62756-351 : Octreotide Acetate 500 ug/ml Intravenous; Subcutaneous Injection, Solution
| NDC: | 62756-351 |
| Labeler: | Sun Pharmaceutical Industries Limited |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Octreotide Acetate |
| Dosage Form: | Intravenous; Subcutaneous Injection, Solution |
| Application #: | ANDA077372 |
| Rev. Date: |
NDC Package Codes:
- 62756-351-44: 10 AMPULE IN 1 PACKAGE (62756‑351‑44) > 1 ML IN 1 AMPULE
Active Ingredients:
- Octreotide Acetate
Dosage Strength:
- 500 ug/mL
Pharmaceutical Classes:
- Somatostatin Analog [EPC]
- Somatostatin Receptor Agonists [MoA]
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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.