43068-610 : PonvoryPonvory Kit


NDC: 43068-610
Labeler: Vanda Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Ponvory
Dosage Form: Kit
Application #: NDA213498
Rev. Date: 


NDC Package Codes:

  • 43068-610-09: 1 KIT IN 1 CARTON (43068‑610‑09) * 1 BLISTER PACK IN 1 CARTON (43068‑606‑00) / 1 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑608‑00) / 1 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑609‑00) / 1 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑607‑00) / 1 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑611‑00) / 3 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑605‑00) / 1 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑604‑00) / 2 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑603‑00) / 2 TABLET, FILM COATED IN 1 BLISTER PACK * 1 BLISTER PACK IN 1 CARTON (43068‑602‑00) / 2 TABLET, FILM COATED IN 1 BLISTER PACK

Related Products:

Based on records with the same trade name.
  • 43068-620 Ponvory 20 mg Oral Tablet, Film Coated by Vanda Pharmaceuticals Inc.
  • 50458-707 PonvoryPonvory Kit by Janssen Pharmaceuticals, Inc
  • 50458-720 Ponvory 20 mg Oral Tablet, Film Coated by Janssen 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.