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OCTREOSCAN
OCTREOSCAN - 0019-9050-40 - (Indium In -111 Pentetreotide)
Drug Information of OCTREOSCAN
| Product NDC: | 0019-9050 |
| Proprietary Name: | OCTREOSCAN |
| Non Proprietary Name: | Indium In -111 Pentetreotide |
| Active Ingredient(s): | & nbsp; Indium In -111 Pentetreotide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OCTREOSCAN
| Product NDC: | 0019-9050 |
| Labeler Name: | Mallinckrodt Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020314 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070501 |
Package Information of OCTREOSCAN
| Package NDC: | 0019-9050-40 |
| Package Description: | 1 KIT in 1 BOX (0019-9050-40) * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS |
NDC Information of OCTREOSCAN
| NDC Code | 0019-9050-40 |
| Proprietary Name | OCTREOSCAN |
| Package Description | 1 KIT in 1 BOX (0019-9050-40) * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS |
| Product NDC | 0019-9050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Indium In -111 Pentetreotide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20070501 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
