succinylcholine chloride

Generic: succinylcholine chloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler zydus lifesciences limited
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride 20 mg/mL

Manufacturer
Zydus Lifesciences Limited

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
depolarizing neuromuscular blocker [epc] neuromuscular depolarizing blockade [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711352
Hyphenated Format 70771-1352

Supplemental Identifiers

RxCUI
1594589
UNII
I9L0DDD30I

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 TRAY (70771-1352-7) / 10 mL in 1 VIAL, MULTI-DOSE (70771-1352-1)
source: ndc

Packages (1)

Ingredients (1)

succinylcholine chloride (20 mg/mL)

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"}