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NEUROLITE
NEUROLITE - 11994-006-02 - (Bicisate dihydrochloride)
Drug Information of NEUROLITE
| Product NDC: | 11994-006 |
| Proprietary Name: | NEUROLITE |
| Non Proprietary Name: | Bicisate dihydrochloride |
| Active Ingredient(s): | & nbsp; Bicisate dihydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NEUROLITE
| Product NDC: | 11994-006 |
| Labeler Name: | Lantheus Medical Imaging, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020256 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19941123 |
Package Information of NEUROLITE
| Package NDC: | 11994-006-02 |
| Package Description: | 2 KIT in 1 PACKAGE, COMBINATION (11994-006-02) > 1 KIT in 1 KIT * 1 mL in 1 VIAL * 1 mL in 1 VIAL |
NDC Information of NEUROLITE
| NDC Code | 11994-006-02 |
| Proprietary Name | NEUROLITE |
| Package Description | 2 KIT in 1 PACKAGE, COMBINATION (11994-006-02) > 1 KIT in 1 KIT * 1 mL in 1 VIAL * 1 mL in 1 VIAL |
| Product NDC | 11994-006 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bicisate dihydrochloride |
| Dosage Form Name | KIT |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19941123 |
| Marketing Category Name | NDA |
| Labeler Name | Lantheus Medical Imaging, Inc. |
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