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Ribavirin
Ribavirin - 68084-150-65 - (Ribavirin)
Drug Information of Ribavirin
| Product NDC: | 68084-150 |
| 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: | 68084-150 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077094 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061130 |
Package Information of Ribavirin
| Package NDC: | 68084-150-65 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (68084-150-65) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-150-11) |
NDC Information of Ribavirin
| NDC Code | 68084-150-65 |
| Proprietary Name | Ribavirin |
| Package Description | 5 BLISTER PACK in 1 CARTON (68084-150-65) > 10 TABLET, FILM COATED in 1 BLISTER PACK (68084-150-11) |
| Product NDC | 68084-150 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ribavirin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20061130 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | RIBAVIRIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
