succinylcholine chloride
Generic: succinylcholine chloride
Labeler: zydus pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
succinylcholine chloride
Generic Name
succinylcholine chloride
Labeler
zydus pharmaceuticals usa inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70710-1377
Product ID
70710-1377_bd190da3-9daf-4859-a431-87c693e18e90
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209467
Listing Expiration
2026-12-31
Marketing Start
2018-05-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707101377
Hyphenated Format
70710-1377
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
ANDA209467 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 TRAY (70710-1377-2) / 10 mL in 1 VIAL, MULTI-DOSE (70710-1377-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "bd190da3-9daf-4859-a431-87c693e18e90", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["017e5ad4-028e-4e34-ac09-d0c8d64c880a"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (70710-1377-2) / 10 mL in 1 VIAL, MULTI-DOSE (70710-1377-1)", "package_ndc": "70710-1377-2", "marketing_start_date": "20180510"}], "brand_name": "Succinylcholine Chloride", "product_id": "70710-1377_bd190da3-9daf-4859-a431-87c693e18e90", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "70710-1377", "generic_name": "Succinylcholine Chloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA209467", "marketing_category": "ANDA", "marketing_start_date": "20180510", "listing_expiration_date": "20261231"}