NDC 0781-3411

Anectine

Succinylcholine Chloride

Anectine is a Intramuscular; Intravenous; Parenteral Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc. The primary component is Succinylcholine Chloride.

Product ID0781-3411_2909fec3-2d00-4750-b2fc-6a1e12706088
NDC0781-3411
Product TypeHuman Prescription Drug
Proprietary NameAnectine
Generic NameSuccinylcholine Chloride
Dosage FormInjection, Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS; PARENTERAL
Marketing Start Date2017-06-22
Marketing CategoryNDA / NDA
Application NumberNDA008453
Labeler NameSandoz Inc
Substance NameSUCCINYLCHOLINE CHLORIDE
Active Ingredient Strength20 mg/mL
Pharm ClassesDepolarizing Neuromuscular Blocker [EPC],Neuromuscular Depolarizing Blockade [PE]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0781-3411-95

10 VIAL, MULTI-DOSE in 1 CARTON (0781-3411-95) > 10 mL in 1 VIAL, MULTI-DOSE (0781-3411-70)
Marketing Start Date2017-06-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0781-3411-95 [00781341195]

Anectine INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA008453
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-06-22

NDC 0781-3411-70 [00781341170]

Anectine INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA008453
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-06-22

Drug Details

Active Ingredients

IngredientStrength
SUCCINYLCHOLINE CHLORIDE20 mg/mL

OpenFDA Data

SPL SET ID:a1e5d29f-111e-4a44-addf-beeb6ea81711
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1594591
  • 1594589
  • Pharmacological Class

    • Depolarizing Neuromuscular Blocker [EPC]
    • Neuromuscular Depolarizing Blockade [PE]

    NDC Crossover Matching brand name "Anectine" or generic name "Succinylcholine Chloride"

    NDCBrand NameGeneric Name
    0781-3009AnectineSuccinylcholine Chloride
    0781-3411AnectineSuccinylcholine Chloride
    0781-9053AnectineSuccinylcholine Chloride
    72572-750AnectineAnectine
    0409-6629QUELICINSuccinylcholine Chloride
    0143-9338Succinylcholine ChlorideSuccinylcholine Chloride
    0404-9960Succinylcholine ChlorideSuccinylcholine Chloride
    0404-9983SUCCINYLCHOLINE CHLORIDEsuccinylcholine chloride
    0548-9801Succinylcholine ChlorideSuccinylcholine Chloride
    0641-6234Succinylcholine ChlorideSuccinylcholine Chloride
    14445-407Succinylcholine ChlorideSuccinylcholine Chloride
    14789-104Succinylcholine ChlorideSuccinylcholine Chloride
    16729-493Succinylcholine ChlorideSuccinylcholine Chloride
    25021-677Succinylcholine ChlorideSuccinylcholine Chloride
    31722-981Succinylcholine ChlorideSuccinylcholine Chloride
    42571-371Succinylcholine ChlorideSuccinylcholine Chloride
    49396-0152Succinylcholine ChlorideSuccinylcholine Chloride

    Trademark Results [Anectine]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ANECTINE
    ANECTINE
    71634029 0576384 Dead/Cancelled
    BURROUGHS WELLCOME & CO. (U. S. A.) INC.
    1952-08-16

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.