Is there a generic for Echothiophate iodide?

The FDA Orange Book does not currently list an approved generic (ANDA) for Echothiophate iodide. It is available as 1 brand (NDA) application.

What is the reference-listed drug for Echothiophate iodide?

PHOSPHOLINE IODIDE (NDA 011963, FERA PHARMS LLC) is the reference-listed drug — the approved product a generic applicant must show its version is the same as.

What dosage forms of Echothiophate iodide are approved?

Echothiophate iodide is approved in the following dosage form: for solution.

FDA Orange Book · active-ingredient family

Echothiophate iodide

Echothiophate iodide is approved in 1 FDA application, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.

Reference-listed drug:PHOSPHOLINE IODIDE · NDA 011963

Brand (NDA)

Generics (ANDA)

Listed patents

Exclusivity periods

Brand (NDA) products · for solution

Product	Applicant	Application	TE	Approved
PHOSPHOLINE IODIDERLD×4	FERA PHARMS LLC	NDA 011963	—	Approved Prior to Jan 1, 1982

Listed patents

No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

Echothiophate iodide — frequently asked questions

Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

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