succinylcholine chloride

Generic: succinylcholine chloride

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler micro labs limited
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride 200 mg/10mL

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-371
Product ID 42571-371_ed051eb0-a20f-20f9-e053-2a95a90af067
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214879
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42571371
Hyphenated Format 42571-371

Supplemental Identifiers

RxCUI
1594589
UPC
0342571371883
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 ANDA214879 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 mg/10mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (42571-371-87) / 10 mL in 1 VIAL, MULTI-DOSE (42571-371-88)
source: ndc

Packages (1)

42571-371-87 25 VIAL, MULTI-DOSE in 1 CARTON (42571-371-87) / 10 mL in 1 VIAL, MULTI-DOSE (42571-371-88)

Ingredients (1)

succinylcholine chloride (200 mg/10mL)

Linked Drug Pages (1)

Succinylcholine Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ed051eb0-a20f-20f9-e053-2a95a90af067", "openfda": {"upc": ["0342571371883"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["204f1c24-4bf6-40d5-95f3-a732db28e033"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (42571-371-87)  / 10 mL in 1 VIAL, MULTI-DOSE (42571-371-88)", "package_ndc": "42571-371-87", "marketing_start_date": "20210301"}], "brand_name": "Succinylcholine Chloride", "product_id": "42571-371_ed051eb0-a20f-20f9-e053-2a95a90af067", "dosage_form": "INJECTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "42571-371", "generic_name": "Succinylcholine Chloride", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "200 mg/10mL"}], "application_number": "ANDA214879", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}