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Ribavirin
Ribavirin - 0781-5177-42 - (Ribavirin)
Drug Information of Ribavirin
| Product NDC: | 0781-5177 |
| Proprietary Name: | Ribavirin |
| Non Proprietary Name: | Ribavirin |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ribavirin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ribavirin
| Product NDC: | 0781-5177 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077743 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061003 |
Package Information of Ribavirin
| Package NDC: | 0781-5177-42 |
| Package Description: | 42 TABLET, FILM COATED in 1 BOTTLE (0781-5177-42) |
NDC Information of Ribavirin
| NDC Code | 0781-5177-42 |
| Proprietary Name | Ribavirin |
| Package Description | 42 TABLET, FILM COATED in 1 BOTTLE (0781-5177-42) |
| Product NDC | 0781-5177 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ribavirin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20061003 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | RIBAVIRIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
