succinylcholine chloride
Generic: succinylcholine chloride
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
succinylcholine chloride
Generic Name
succinylcholine chloride
Labeler
zydus lifesciences limited
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
succinylcholine chloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1352
Product ID
70771-1352_88c956e8-67e6-40b2-8b44-2d21e0e5fcf6
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
707711352
Hyphenated Format
70771-1352
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 (70771-1352-7) / 10 mL in 1 VIAL, MULTI-DOSE (70771-1352-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "88c956e8-67e6-40b2-8b44-2d21e0e5fcf6", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["c7f409ed-e4f4-4cd6-8f37-93f505dd986d"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (70771-1352-7) / 10 mL in 1 VIAL, MULTI-DOSE (70771-1352-1)", "package_ndc": "70771-1352-7", "marketing_start_date": "20180510"}], "brand_name": "Succinylcholine Chloride", "product_id": "70771-1352_88c956e8-67e6-40b2-8b44-2d21e0e5fcf6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "70771-1352", "generic_name": "Succinylcholine Chloride", "labeler_name": "Zydus Lifesciences Limited", "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"}