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Octreotide Acetate
Octreotide Acetate - 67457-239-01 - (octreotide acetate)
Drug Information of Octreotide Acetate
| Product NDC: | 67457-239 |
| Proprietary Name: | Octreotide Acetate |
| Non Proprietary Name: | octreotide acetate |
| Active Ingredient(s): | 50 ug/mL & nbsp; octreotide acetate |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Octreotide Acetate
| Product NDC: | 67457-239 |
| Labeler Name: | Mylan Institutional LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079198 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130425 |
Package Information of Octreotide Acetate
| Package NDC: | 67457-239-01 |
| Package Description: | 10 SYRINGE in 1 CARTON (67457-239-01) > 1 mL in 1 SYRINGE (67457-239-00) |
NDC Information of Octreotide Acetate
| NDC Code | 67457-239-01 |
| Proprietary Name | Octreotide Acetate |
| Package Description | 10 SYRINGE in 1 CARTON (67457-239-01) > 1 mL in 1 SYRINGE (67457-239-00) |
| Product NDC | 67457-239 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | octreotide acetate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS; SUBCUTANEOUS |
| Start Marketing Date | 20130425 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional LLC |
| Substance Name | OCTREOTIDE ACETATE |
| Strength Number | 50 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA] |
