Orange Book product · Brand (NDA)

PRALIDOXIME CHLORIDE (AUTOINJECTOR)

PRALIDOXIME CHLORIDE

Brand (NDA)NDA 018986DISCN MERIDIAN MEDCL TECHN

View PRALIDOXIME CHLORIDE family Open on FDA Orange Book

At a glance

Apr 26, 1983

Approved

Brand (NDA)

Application

Not listed

TE code

None

Listed patents

Key dates

Approval
FDA approval date of this drug product.
Apr 26, 1983
43 yr 9 mo ago
Today

Pharmaceutical detail

Active ingredient

PRALIDOXIME CHLORIDE

Strength

600MG/2ML (300MG/ML)

Dosage form

SOLUTION

Route

INTRAMUSCULAR

TE code

Not listed

Application

NDA 018986

Product number

001

Marketing status

DISCN

Reference listed drug (RLD)

Yes

Reference standard (RS)

Active-ingredient family

View full family

This is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

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.

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