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RIBASPHERE RibaPak
RIBASPHERE RibaPak - 66435-105-99 - (ribavirin)
Drug Information of RIBASPHERE RibaPak
| Product NDC: | 66435-105 |
| Proprietary Name: | RIBASPHERE RibaPak |
| Non Proprietary Name: | ribavirin |
| Active Ingredient(s): | 400 mg/1 & nbsp; ribavirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RIBASPHERE RibaPak
| Product NDC: | 66435-105 |
| Labeler Name: | Kadmon Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077456 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100101 |
Package Information of RIBASPHERE RibaPak
| Package NDC: | 66435-105-99 |
| Package Description: | 4 DOSE PACK in 1 CARTON (66435-105-99) > 14 TABLET in 1 DOSE PACK (66435-105-56) |
NDC Information of RIBASPHERE RibaPak
| NDC Code | 66435-105-99 |
| Proprietary Name | RIBASPHERE RibaPak |
| Package Description | 4 DOSE PACK in 1 CARTON (66435-105-99) > 14 TABLET in 1 DOSE PACK (66435-105-56) |
| Product NDC | 66435-105 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ribavirin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | ANDA |
| Labeler Name | Kadmon Pharmaceuticals, LLC |
| Substance Name | RIBAVIRIN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
