0074-3239 : Moderiba 400 mg/1 Oral Tablet, Film Coated
| NDC: | 0074-3239 |
| Labeler: | Abbvie Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Moderiba |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA077456 |
| Rev. Date: |
Appearance:
| Markings: | 400;3RP |
| Shapes: |
Oval |
| Colors: |
 Blue |
| Size (mm): | 18 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 0074-3239-56: 4 DOSE PACK IN 1 CARTON (0074‑3239‑56) > 14 TABLET, FILM COATED IN 1 DOSE PACK (0074‑3239‑14)
Active Ingredients:
- Ribavirin
Dosage Strength:
- 400 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Lactose Monohydrate
- Croscarmellose Sodium
- Povidones
- Magnesium Stearate
- Water
- Polyvinyl Alcohol
- Titanium Dioxide
- Polyethylene Glycol 3350
- Talc
- Fd&c Blue No. 1
- Carnauba Wax
Pharmaceutical Classes:
- Nucleoside Analog [Chemical/Ingredient]
- Nucleoside Analog Antiviral [EPC]
Related Products:
Based on records with the same trade name.- 0074-3197 Moderiba 200 mg/1 Oral Tablet, Film Coated by Abbvie Inc.
- 0074-3224 Moderiba Kit by Abbvie Inc.
- 0074-3271 Moderiba Kit by Abbvie Inc.
- 0074-3282 Moderiba 600 mg/1 Oral Tablet, Film Coated by Abbvie Inc.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.