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Orange Book product · Brand (NDA)

Anectine

Succinylcholine Chloride

Brand (NDA)NDA 008453Discontinued Sandoz
Approved
Approved Prior to Jan 1, 1982
Application
Brand (NDA)
TE code
Not listed
Listed patents
0
Anectine (Succinylcholine Chloride) is Sandoz's brand-name drug, approved by the FDA under NDA 008453. Its marketing status is listed as discontinued; a discontinued listing is not, by itself, a finding that the drug was withdrawn for safety or effectiveness. 29 approved generics share this drug's active ingredient.

Sourced from the FDA Orange Book

Approval, patents, exclusivity

Key dates

Key dates

No patent or exclusivity dates are listed for this product.

FDA product record

Pharmaceutical detail

Pharmaceutical detail

Active ingredient

SUCCINYLCHOLINE CHLORIDE

Strength

1GM/VIAL

Dosage form

INJECTABLE

Route

INJECTION

TE code

Not listed

Application

NDA 008453

Product number

004

Marketing status

Discontinued

Reference listed drug (RLD)

No

Reference standard (RS)

No

Same application

Other strengths in NDA 008453

Brand + generics

Active-ingredient family

Orange Book patent file

Listed patents

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.

Anectine — frequently asked questions

Approval, therapeutic equivalence, patents, and exclusivity for this product, from the FDA Orange Book.

Built directly from the FDA Orange Book data file. This product page links back to the Succinylcholine Chloride active-ingredient family, which is the canonical reference for generics, patents, and exclusivity across all strengths.

Related FDA reference tools

Agent CTA Background

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