68462-895 : Varenicline TartrateVarenicline Tartrate Kit


NDC: 68462-895
Labeler: Glenmark Pharmaceuticals Inc., USA
Product Type: Human Prescription Drug
Drug Name:  Varenicline Tartrate
Dosage Form: Kit
Application #: ANDA214255
Rev. Date: 


NDC Package Codes:

  • 68462-895-04: 1 KIT IN 1 CARTON (68462‑895‑04) * 11 TABLET, FILM COATED IN 1 BLISTER PACK * 42 TABLET, FILM COATED IN 1 BLISTER PACK

Related Products:

Based on records with the same trade name.
  • 68462-893 Varenicline Tartrate .5 mg Oral Tablet, Film Coated by Glenmark Pharmaceuticals Inc., USA
  • 68462-894 Varenicline Tartrate 1 mg Oral Tablet, Film Coated by Glenmark Pharmaceuticals Inc., USA
  • 42934-104 Varenicline Tartrate .5 mg/561 Oral Tablet, Film Coated by Medley Pharmaceuticals Limited
  • 42934-105 Varenicline Tartrate 1 mg/561 Oral Tablet, Film Coated by Medley Pharmaceuticals Limited
  • 42934-106 Varenicline TartrateVarenicline Tartrate Oral Kit by Medley Pharmaceuticals Limited
  • 69315-402 Varenicline Tartrate .5 mg/561 Oral Tablet, Film Coated by Leading Pharma, LLC
  • 69315-403 Varenicline Tartrate 1 mg/561 Oral Tablet, Film Coated by Leading Pharma, LLC
  • 69315-404 Varenicline TartrateVarenicline Tartrate Kit by Leading Pharma, LLC
  • 70748-125 Varenicline TartrateVarenicline Tartrate Kit by Lupin Pharmaceuticals, 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.