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Sandostatin LAR Depot
Sandostatin LAR Depot - 0078-0341-61 - (octreotide acetate)
Drug Information of Sandostatin LAR Depot
| Product NDC: | 0078-0341 |
| Proprietary Name: | Sandostatin LAR Depot |
| Non Proprietary Name: | octreotide acetate |
| Active Ingredient(s): | & nbsp; octreotide acetate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sandostatin LAR Depot
| Product NDC: | 0078-0341 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021008 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19881101 |
Package Information of Sandostatin LAR Depot
| Package NDC: | 0078-0341-61 |
| Package Description: | 1 KIT in 1 KIT (0078-0341-61) * 2.5 mL in 1 SYRINGE * 1 SWAB in 1 PACKAGE * 5 mL in 1 VIAL, SINGLE-USE |
NDC Information of Sandostatin LAR Depot
| NDC Code | 0078-0341-61 |
| Proprietary Name | Sandostatin LAR Depot |
| Package Description | 1 KIT in 1 KIT (0078-0341-61) * 2.5 mL in 1 SYRINGE * 1 SWAB in 1 PACKAGE * 5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0078-0341 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | octreotide acetate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19881101 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
