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VIVITROL
VIVITROL - 65757-301-01 - (naltrexone)
Drug Information of VIVITROL
| Product NDC: | 65757-301 |
| Proprietary Name: | VIVITROL |
| Non Proprietary Name: | naltrexone |
| Active Ingredient(s): | & nbsp; naltrexone |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VIVITROL
| Product NDC: | 65757-301 |
| Labeler Name: | Alkermes, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021897 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060613 |
Package Information of VIVITROL
| Package NDC: | 65757-301-01 |
| Package Description: | 1 KIT in 1 CARTON (65757-301-01) * 4 mL in 1 VIAL, GLASS (65757-303-02) * 4 mL in 1 VIAL, GLASS (65757-305-03) |
NDC Information of VIVITROL
| NDC Code | 65757-301-01 |
| Proprietary Name | VIVITROL |
| Package Description | 1 KIT in 1 CARTON (65757-301-01) * 4 mL in 1 VIAL, GLASS (65757-303-02) * 4 mL in 1 VIAL, GLASS (65757-305-03) |
| Product NDC | 65757-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | naltrexone |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20060613 |
| Marketing Category Name | NDA |
| Labeler Name | Alkermes, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
