anectine
Generic: succinylcholine chloride
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
anectine
Generic Name
succinylcholine chloride
Labeler
sandoz inc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-9053
Product ID
0781-9053_24ab36dd-dc6b-4207-a5a9-25c6c60df8dc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA008453
Listing Expiration
2026-12-31
Marketing Start
2019-06-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07819053
Hyphenated Format
0781-9053
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
anectine (source: ndc)
Generic Name
succinylcholine chloride (source: ndc)
Application Number
NDA008453 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 10 VIAL, MULTI-DOSE in 1 CARTON (0781-9053-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-9053-70)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "PARENTERAL"], "spl_id": "24ab36dd-dc6b-4207-a5a9-25c6c60df8dc", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589", "1594591"], "spl_set_id": ["04a4e6f5-6fa1-42e1-a3f9-21fca7786b15"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (0781-9053-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-9053-70)", "package_ndc": "0781-9053-95", "marketing_start_date": "20190612"}], "brand_name": "Anectine", "product_id": "0781-9053_24ab36dd-dc6b-4207-a5a9-25c6c60df8dc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "0781-9053", "generic_name": "Succinylcholine Chloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anectine", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "NDA008453", "marketing_category": "NDA", "marketing_start_date": "20190612", "listing_expiration_date": "20261231"}