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NDC 65862-0207-05 Ribavirin 200 mg/1 Details
Ribavirin 200 mg/1
Ribavirin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is RIBAVIRIN.
MedlinePlus Drug Summary
Ribavirin is used with an interferon medication such as peginterferon alfa-2a [Pegasys] or peginterferon alpha-2b [PEG-Intron]) to treat hepatitis C in people who have not been treated with an interferon before. Ribavirin is in a class of antiviral medications called nucleoside analogues. It works by stopping the virus that causes hepatitis C from spreading inside the body. It is not known if treatment that includes ribavirin and another medication cures hepatitis C infection, prevents liver damage that may be caused by hepatitis C, or prevents the spread of hepatitis C to other people.
Related Packages: 65862-0207-05Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ribavirin
Product Information
| NDC | 65862-0207 |
|---|---|
| Product ID | 65862-207_1df6353a-6bb8-4b76-8c41-c9d97b05b4c3 |
| Associated GPIs | 12353070000320 |
| GCN Sequence Number | 051637 |
| GCN Sequence Number Description | ribavirin TABLET 200 MG ORAL |
| HIC3 | W5G |
| HIC3 Description | HEPATITIS C TREATMENT AGENTS |
| GCN | 18969 |
| HICL Sequence Number | 004184 |
| HICL Sequence Number Description | RIBAVIRIN |
| Brand/Generic | Generic |
| Proprietary Name | Ribavirin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ribavirin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 200 |
| Active Ingredient Units | mg/1 |
| Substance Name | RIBAVIRIN |
| Labeler Name | Aurobindo Pharma Limited |
| Pharmaceutical Class | Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA079111 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65862-0207-05 (65862020705)
| NDC Package Code | 65862-207-05 |
|---|---|
| Billing NDC | 65862020705 |
| Package | 500 TABLET, FILM COATED in 1 BOTTLE (65862-207-05) |
| Marketing Start Date | 2009-09-17 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |