Product Details for NDA 011963
PHOSPHOLINE IODIDE (ECHOTHIOPHATE IODIDE)
0.125%
Marketing Status: Prescription
0.03%
Marketing Status: Discontinued
0.06%
Marketing Status: Discontinued
0.25%
Marketing Status: Discontinued
0.125%
Marketing Status: Prescription
Active Ingredient: ECHOTHIOPHATE IODIDE
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.125%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N011963
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
PHOSPHOLINE IODIDE (ECHOTHIOPHATE IODIDE)
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.125%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N011963
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Prescription
Patent and Exclusivity Information
0.03%
Marketing Status: Discontinued
Active Ingredient: ECHOTHIOPHATE IODIDE
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.03%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011963
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
PHOSPHOLINE IODIDE (ECHOTHIOPHATE IODIDE)
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.03%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011963
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.06%
Marketing Status: Discontinued
Active Ingredient: ECHOTHIOPHATE IODIDE
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.06%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011963
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
PHOSPHOLINE IODIDE (ECHOTHIOPHATE IODIDE)
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.06%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011963
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.25%
Marketing Status: Discontinued
Active Ingredient: ECHOTHIOPHATE IODIDE
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.25%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011963
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: PHOSPHOLINE IODIDE
Dosage Form; Route of Administration: FOR SOLUTION; OPHTHALMIC
Strength: 0.25%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011963
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: FERA PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information