succinylcholine chloride

Generic: succinylcholine chloride

Labeler: be pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name succinylcholine chloride
Generic Name succinylcholine chloride
Labeler be pharmaceuticals inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

succinylcholine chloride 20 mg/mL

Manufacturer
BE Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71839-121
Product ID 71839-121_200064fa-2d8d-40ac-92a2-cba54deef1c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216003
Listing Expiration 2026-12-31
Marketing Start 2022-02-07

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71839121
Hyphenated Format 71839-121

Supplemental Identifiers

RxCUI
1594589
UPC
0371839121014
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 ANDA216003 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25) / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)
source: ndc

Packages (1)

71839-121-25 25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25) / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)

Ingredients (1)

succinylcholine chloride (20 mg/mL)

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": "200064fa-2d8d-40ac-92a2-cba54deef1c9", "openfda": {"upc": ["0371839121014"], "unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["6e6e0ce7-c73c-407f-9678-724425f24976"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25)  / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01)", "package_ndc": "71839-121-25", "marketing_start_date": "20220207"}], "brand_name": "Succinylcholine Chloride", "product_id": "71839-121_200064fa-2d8d-40ac-92a2-cba54deef1c9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "71839-121", "generic_name": "Succinylcholine Chloride", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA216003", "marketing_category": "ANDA", "marketing_start_date": "20220207", "listing_expiration_date": "20261231"}