42291-414 : Famciclovir 125 mg Oral Tablet, Film Coated


NDC: 42291-414
Labeler: Avkare
Product Type: Human Prescription Drug
Drug Name:  Famciclovir
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA077487
Rev. Date: 


NDC Package Codes:

  • 42291-414-30: 30 TABLET, FILM COATED IN 1 BOTTLE (42291‑414‑30)

Active Ingredients:

  • Famciclovir

Dosage Strength:

  • 125 mg

Pharmaceutical Classes:

  • DNA Polymerase Inhibitors [MoA]
  • Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
  • Nucleoside Analog [EXT]

Related Products:

Based on records with the same trade name.
  • 42291-415 Famciclovir 250 mg Oral Tablet, Film Coated by Avkare
  • 42291-416 Famciclovir 500 mg Oral Tablet, Film Coated by Avkare
  • 42291-275 Famciclovir 125 mg Oral Tablet by Avkare, Inc.
  • 42291-276 Famciclovir 250 mg Oral Tablet by Avkare, Inc.
  • 42291-277 Famciclovir 500 mg Oral Tablet by Avkare, Inc.
  • 0054-0196 Famciclovir 125 mg Oral Tablet by Roxane Laboratories, Inc.
  • 0054-0197 Famciclovir 250 mg Oral Tablet by Roxane Laboratories, Inc.
  • 0054-0198 Famciclovir 500 mg Oral Tablet by Roxane Laboratories, Inc.
  • 0093-8117 Famciclovir 125 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-8118 Famciclovir 250 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0093-8119 Famciclovir 500 mg Oral Tablet by Teva Pharmaceuticals USA Inc
  • 0378-4490 Famciclovir 125 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0378-4491 Famciclovir 250 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0378-4492 Famciclovir 500 mg Oral Tablet by Mylan Pharmaceuticals Inc.
  • 0591-3271 Famciclovir 125 mg Oral Tablet by Watson Laboratories, Inc.
  • 0591-3272 Famciclovir 250 mg Oral Tablet by Watson Laboratories, Inc.
  • 0591-3273 Famciclovir 500 mg Oral Tablet by Watson Laboratories, Inc.
  • 0781-5620 Famciclovir 125 mg Oral Tablet by Sandoz Inc
  • 0781-5621 Famciclovir 250 mg Oral Tablet by Sandoz Inc
  • 0781-5622 Famciclovir 500 mg Oral Tablet by Sandoz Inc
  • More related products ...

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.