NDC 0409-6629

QUELICIN

Succinylcholine Chloride

QUELICIN is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Succinylcholine Chloride.

• Product ID: 0409-6629_26d36f80-bc3b-48b4-a715-38a2759698cf
• NDC: 0409-6629
• Product Type: Human Prescription Drug
• Proprietary Name: QUELICIN
• Generic Name: Succinylcholine Chloride
• Dosage Form: Injection, Solution
• Route of Administration: INTRAMUSCULAR; INTRAVENOUS
• Marketing Start Date: 2005-04-30
• Marketing Category: NDA / NDA
• Application Number: NDA008845
• Labeler Name: Hospira, Inc.
• Substance Name: SUCCINYLCHOLINE CHLORIDE
• Active Ingredient Strength: 20 mg/mL
• Pharm Classes: Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0409-6629-02

25 VIAL, MULTI-DOSE in 1 TRAY (0409-6629-02) > 10 mL in 1 VIAL, MULTI-DOSE (0409-6629-12)

• Marketing Start Date: 2005-04-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0409-6629-02 [00409662902]

QUELICIN INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA008845
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2005-04-30

NDC 0409-6629-61 [00409662961]

QUELICIN INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA008845
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2010-10-11
• Marketing End Date: 2014-06-05

NDC 0409-6629-12 [00409662912]

QUELICIN INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA008845
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2019-10-11

NDC 0409-6629-25 [00409662925]

QUELICIN INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA008845
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2014-03-31

NDC 0409-6629-35 [00409662935]

QUELICIN INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA008845
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2019-05-08

Drug Details

Active Ingredients

Ingredient	Strength
SUCCINYLCHOLINE CHLORIDE	20 mg/mL

OpenFDA Data

• SPL SET ID: c06156ae-b889-4250-bc85-1435b2635829
• Manufacturer:
  • Hospira, Inc.
• UNII:
  • I9L0DDD30I
• RxNorm Concept Unique ID - RxCUI:
  • 1594593
  • 1594589

Pharmacological Class

• Depolarizing Neuromuscular Blocker [EPC]
• Neuromuscular Depolarizing Blockade [PE]

NDC Crossover Matching brand name "QUELICIN" or generic name "Succinylcholine Chloride"

NDC	Brand Name	Generic Name
0409-6629	QUELICIN	Succinylcholine Chloride
71872-7026	Quelicin	Quelicin
71872-7146	Quelicin	Quelicin
0781-3009	Anectine	Succinylcholine Chloride
0781-3411	Anectine	Succinylcholine Chloride
0781-9053	Anectine	Succinylcholine Chloride
0143-9338	Succinylcholine Chloride	Succinylcholine Chloride
0404-9960	Succinylcholine Chloride	Succinylcholine Chloride
0404-9983	SUCCINYLCHOLINE CHLORIDE	succinylcholine chloride
0548-9801	Succinylcholine Chloride	Succinylcholine Chloride
0641-6234	Succinylcholine Chloride	Succinylcholine Chloride
14445-407	Succinylcholine Chloride	Succinylcholine Chloride
14789-104	Succinylcholine Chloride	Succinylcholine Chloride
16729-493	Succinylcholine Chloride	Succinylcholine Chloride
25021-677	Succinylcholine Chloride	Succinylcholine Chloride
31722-981	Succinylcholine Chloride	Succinylcholine Chloride
42571-371	Succinylcholine Chloride	Succinylcholine Chloride
49396-0152	Succinylcholine Chloride	Succinylcholine Chloride