0046-1065 : Phospholine Iodide Kit


NDC: 0046-1065
Labeler: Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
Product Type: Human Prescription Drug
Drug Name:  Phospholine Iodide Ophthalmic
Dosage Form: Kit
Application #: NDA011963
Rev. Date: 


NDC Package Codes:

  • 0046-1065-05: 1 KIT IN 1 KIT (0046‑1065‑05) * 6.25 ML IN 1 BOTTLE (0046‑1465‑05) * 5 ML IN 1 BOTTLE (0046‑1162‑05)

Active Ingredients:

  • Echothiophate Iodide

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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.