0078-0366 : Famvir 125 mg Oral Tablet
NDC: | 0078-0366 |
Labeler: | Novartis Pharmaceuticals Corporation |
Product Type: | Human Prescription Drug |
Drug Name: | Famvir |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | NDA020363 |
Rev. Date: |
Appearance:
Markings: | FAMVIR;125 |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 8 |
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. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 0078-0366-15: 30 TABLET, FILM COATED IN 1 BOTTLE (0078‑0366‑15)
Active Ingredients:
- Famciclovir
Dosage Strength:
- 125 mg
Inactive Ingredients:
- Hydroxypropyl Cellulose (Type H)
- Lactose
- Magnesium Stearate
- Polyethylene Glycols
- Sodium Starch Glycolate Type a Potato
- Titanium Dioxide
Pharmaceutical Classes:
- DNA Polymerase Inhibitors [MoA]
- Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
- Nucleoside Analog [Chemical/Ingredient]
Related Products:
Based on records with the same trade name.- 0078-0367 Famvir 250 mg Oral Tablet by Novartis Pharmaceuticals Corporation
- 0078-0368 Famvir 500 mg Oral Tablet by Novartis Pharmaceuticals Corporation
NDC QR Code
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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.