27241-159 : Valganciclovir Hydrochloride 50 mg/ml Oral Powder, for Solution


NDC: 27241-159
Labeler: Ajanta Pharma Limited
Product Type: Human Prescription Drug
Drug Name:  Valganciclovir Hydrochloride
Dosage Form: Oral Powder, for Solution
Application #: ANDA212890
Rev. Date: 


NDC Package Codes:

  • 27241-159-19: 1 POUCH IN 1 CARTON (27241‑159‑19) > 1 BOTTLE IN 1 POUCH > 100 ML IN 1 BOTTLE

Active Ingredients:

  • Valganciclovir Hydrochloride

Dosage Strength:

  • 50 mg/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 43598-356 Valganciclovir Hydrochloride 450 mg Oral Tablet by Dr. Reddy's Laboratories Inc
  • 63739-357 Valganciclovir Hydrochloride 450 mg Oral Tablet by Mckesson Corporation
  • 65862-753 Valganciclovir Hydrochloride 450 mg Oral Tablet by Aurobindo Pharma Limited
  • 70010-051 Valganciclovir Hydrochloride Hydrochloride 50 mg/ml Oral for Solution by Granules Pharmaceuticals Inc.
  • 70069-810 Valganciclovir Hydrochloride Hydrochloride 50 mg/ml Oral for Solution by Somerset Therapeutics, LLC
  • 72205-019 Valganciclovir Hydrochloride 50 mg/ml Oral for Solution by Novadoz Pharmaceuticals LLC

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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.