Anectine
Succinylcholine Chloride
Sourced from the FDA Orange Book
Key dates
Key dates
No patent or exclusivity dates are listed for this product.
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
Other strengths in NDA 008453
Active-ingredient family
This is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 2021Succinylcholine ChlorideBrand (NDA)
NDA 215143 · Hikma
- —QuelicinBrand (NDA)
NDA 008845 · Hospira
- —SucostrinBrand (NDA)
NDA 008847 · Apothecon
- 2025Succinylcholine ChlorideGeneric (ANDA)
ANDA 217885 · Fresenius Kabi USA
- 2025Succinylcholine ChlorideGeneric (ANDA)
ANDA 217884 · Fresenius Kabi USA
- 2024Succinylcholine ChlorideGeneric (ANDA)
ANDA 218878 · Baxter Hlthcare Corp
- 2024Succinylcholine ChlorideGeneric (ANDA)
ANDA 217873 · Steriscience
- 2024Succinylcholine ChlorideGeneric (ANDA)
ANDA 218467 · DR Reddys
- 2023Succinylcholine ChlorideGeneric (ANDA)
ANDA 217808 · Eugia Pharma
- 2023Succinylcholine ChlorideGeneric (ANDA)
ANDA 216127 · Mankind Pharma
- 2022Succinylcholine ChlorideGeneric (ANDA)
ANDA 216003 · Be Pharms
- 2021Succinylcholine ChlorideGeneric (ANDA)
ANDA 214514 · Meitheal
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
- FDA Purple BookLicensed biologics, biosimilars, interchangeables, BLA records, and exclusivity dates.
- FDA BiosimilarsThe list of FDA-approved biosimilars and interchangeable biosimilars, by reference product.
- 510(k) Predicate DatabaseSearch FDA 510(k) clearances and map predicate-device lineage.
- FDA 483 & Inspection DatabaseFDA Form 483 observations and inspection records by firm, date, and citation.

