0093-8210 : FinzalaFinzala Kit


NDC: 0093-8210
Labeler: Teva Pharmaceuticals USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Finzala
Dosage Form: Kit
Application #: ANDA210087
Rev. Date: 


NDC Package Codes:

  • 0093-8210-62: 3 POUCH IN 1 CARTON (0093‑8210‑62) > 1 BLISTER PACK IN 1 POUCH (0093‑8210‑28) > 1 KIT IN 1 BLISTER PACK * 24 TABLET, CHEWABLE IN 1 BLISTER PACK (0093‑3476‑38) * 4 TABLET IN 1 BLISTER PACK (0093‑3525‑44)

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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.