NDC 0046-1065

Phospholine Iodide Ophthalmic

Echothiophate Iodide

Phospholine Iodide Ophthalmic is a Kit in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is .

Product ID0046-1065_635103d6-993d-48c1-9c2b-b69d5f34032b
NDC0046-1065
Product TypeHuman Prescription Drug
Proprietary NamePhospholine Iodide Ophthalmic
Generic NameEchothiophate Iodide
Dosage FormKit
Marketing Start Date1959-12-04
Marketing CategoryNDA / NDA
Application NumberNDA011963
Labeler NameWyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 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)
Marketing Start Date1959-12-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0046-1065-05 [00046106505]

Phospholine Iodide Ophthalmic KIT
Marketing CategoryNDA
Application NumberNDA011963
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1959-12-04

Drug Details

OpenFDA Data

SPL SET ID:e4bb53c7-9061-43fc-878f-dc1b19801bfc
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 205739
  • 310049

  • Trademark Results [Phospholine Iodide]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PHOSPHOLINE IODIDE
    PHOSPHOLINE IODIDE
    72087782 0704866 Live/Registered
    CAMPBELL PHARMAMEUTICALS, INC.
    1959-12-22

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