succinylcholine chloride

Generic: succinylcholine chloride

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

Drug Facts

Product Profile

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

succinylcholine chloride 20 mg/mL

Manufacturer
Amring Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 69918-700
Product ID 69918-700_6b0dd7d4-8a1d-40b7-8116-793ce6f06a18
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210231
Listing Expiration 2026-12-31
Marketing Start 2019-04-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69918700
Hyphenated Format 69918-700

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 ANDA210231 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 VIAL, MULTI-DOSE in 1 CARTON (69918-700-10) / 10 mL in 1 VIAL, MULTI-DOSE (69918-700-01)
  • 25 VIAL, MULTI-DOSE in 1 CARTON (69918-700-25) / 10 mL in 1 VIAL, MULTI-DOSE (69918-700-01)
source: ndc

Packages (2)

69918-700-10 10 VIAL, MULTI-DOSE in 1 CARTON (69918-700-10) / 10 mL in 1 VIAL, MULTI-DOSE (69918-700-01) 69918-700-25 25 VIAL, MULTI-DOSE in 1 CARTON (69918-700-25) / 10 mL in 1 VIAL, MULTI-DOSE (69918-700-01)

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": "6b0dd7d4-8a1d-40b7-8116-793ce6f06a18", "openfda": {"unii": ["I9L0DDD30I"], "rxcui": ["1594589"], "spl_set_id": ["23bb29da-55a6-4f06-b3a4-2f7b65ec5909"], "manufacturer_name": ["Amring Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (69918-700-10)  / 10 mL in 1 VIAL, MULTI-DOSE (69918-700-01)", "package_ndc": "69918-700-10", "marketing_start_date": "20190410"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (69918-700-25)  / 10 mL in 1 VIAL, MULTI-DOSE (69918-700-01)", "package_ndc": "69918-700-25", "marketing_start_date": "20190410"}], "brand_name": "Succinylcholine Chloride", "product_id": "69918-700_6b0dd7d4-8a1d-40b7-8116-793ce6f06a18", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Depolarizing Neuromuscular Blocker [EPC]", "Neuromuscular Depolarizing Blockade [PE]"], "product_ndc": "69918-700", "generic_name": "Succinylcholine Chloride", "labeler_name": "Amring Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Succinylcholine Chloride", "active_ingredients": [{"name": "SUCCINYLCHOLINE CHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA210231", "marketing_category": "ANDA", "marketing_start_date": "20190410", "listing_expiration_date": "20261231"}