succinylcholine chloride
Generic: succinylcholine chloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
succinylcholine chloride
Generic Name
succinylcholine chloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride dihydrate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9338
Product ID
0143-9338_07245c04-4789-4b91-9f5e-ab55726042e6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213229
Listing Expiration
2026-12-31
Marketing Start
2021-04-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439338
Hyphenated Format
0143-9338
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
succinylcholine chloride (source: ndc)
Generic Name
succinylcholine chloride (source: ndc)
Application Number
ANDA213229 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 25 VIAL in 1 CARTON (0143-9338-25) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "07245c04-4789-4b91-9f5e-ab55726042e6", "openfda": {"unii": ["8L0S1G435E"], "rxcui": ["1594589"], "spl_set_id": ["488e1689-84d4-4f96-ac85-fa0cbc661cb6"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0143-9338-25) / 10 mL in 1 VIAL", "package_ndc": "0143-9338-25", "marketing_start_date": "20210426"}], "brand_name": "Succinylcholine Chloride", "product_id": "0143-9338_07245c04-4789-4b91-9f5e-ab55726042e6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "0143-9338", "generic_name": "Succinylcholine Chloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE DIHYDRATE", "strength": "20 mg/mL"}], "application_number": "ANDA213229", "marketing_category": "ANDA", "marketing_start_date": "20210426", "listing_expiration_date": "20261231"}