Product NDC: | 66435-101 |
Proprietary Name: | Ribasphere |
Non Proprietary Name: | Ribavirin |
Active Ingredient(s): | 200 mg/1 & nbsp; Ribavirin |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66435-101 |
Labeler Name: | Kadmon Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076203 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040407 |
Package NDC: | 66435-101-70 |
Package Description: | 70 CAPSULE in 1 BOTTLE, PLASTIC (66435-101-70) |
NDC Code | 66435-101-70 |
Proprietary Name | Ribasphere |
Package Description | 70 CAPSULE in 1 BOTTLE, PLASTIC (66435-101-70) |
Product NDC | 66435-101 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ribavirin |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20040407 |
Marketing Category Name | ANDA |
Labeler Name | Kadmon Pharmaceuticals, LLC |
Substance Name | RIBAVIRIN |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |