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 ID: 0046-1065_635103d6-993d-48c1-9c2b-b69d5f34032b
• NDC: 0046-1065
• Product Type: Human Prescription Drug
• Proprietary Name: Phospholine Iodide Ophthalmic
• Generic Name: Echothiophate Iodide
• Dosage Form: Kit
• Marketing Start Date: 1959-12-04
• Marketing Category: NDA / NDA
• Application Number: NDA011963
• Labeler Name: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

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 Date: 1959-12-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0046-1065-05 [00046106505]

Phospholine Iodide Ophthalmic KIT

• Marketing Category: NDA
• Application Number: NDA011963
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1959-12-04

Drug Details

OpenFDA Data

• SPL SET ID: e4bb53c7-9061-43fc-878f-dc1b19801bfc
• Manufacturer:
  • Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 205739
  • 310049