NDC 63323-781

Vecuronium Bromide

Vecuronium Bromide

Vecuronium Bromide is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Vecuronium Bromide.

• Product ID: 63323-781_19b712c5-7fb2-435c-aa19-6e63fd1ced39
• NDC: 63323-781
• Product Type: Human Prescription Drug
• Proprietary Name: Vecuronium Bromide
• Generic Name: Vecuronium Bromide
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2016-06-30
• Marketing Category: ANDA / ANDA
• Application Number: ANDA205390
• Labeler Name: Fresenius Kabi USA, LLC
• Substance Name: VECURONIUM BROMIDE
• Active Ingredient Strength: 1 mg/mL
• Pharm Classes: Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 63323-781-44

10 VIAL in 1 CARTON (63323-781-44) > 10 mL in 1 VIAL (63323-781-41)

• Marketing Start Date: 2016-06-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63323-781-21 [63323078121]

Vecuronium Bromide INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA205390
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-02-27

NDC 63323-781-44 [63323078144]

Vecuronium Bromide INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA205390
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-06-30

NDC 63323-781-41 [63323078141]

Vecuronium Bromide INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA205390
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-06-30

NDC 63323-781-10 [63323078110]

Vecuronium Bromide INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA205390
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-06-30

Drug Details

Active Ingredients

Ingredient	Strength
VECURONIUM BROMIDE	1 mg/mL

OpenFDA Data

• SPL SET ID: d3163bdf-f163-41b5-a38a-3cd6fc1a50ba
• Manufacturer:
  • Fresenius Kabi USA, LLC
• UNII:
  • 7E4PHP5N1D
• RxNorm Concept Unique ID - RxCUI:
  • 859437

Pharmacological Class

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

NDC Crossover Matching brand name "Vecuronium Bromide" or generic name "Vecuronium Bromide"

NDC	Brand Name	Generic Name
0143-9232	Vecuronium Bromide	Vecuronium Bromide
0143-9234	Vecuronium Bromide	Vecuronium Bromide
0409-1632	Vecuronium Bromide	Vecuronium Bromide
0409-1634	Vecuronium Bromide	Vecuronium Bromide
0703-2914	Vecuronium Bromide	Vecuronium Bromide
0703-2925	Vecuronium Bromide	Vecuronium Bromide
23360-160	Vecuronium bromide	Vecuronium bromide
47335-931	vecuronium bromide	vecuronium bromide
47335-932	vecuronium bromide	vecuronium bromide
51662-1475	VECURONIUM BROMIDE	VECURONIUM BROMIDE
51662-1547	VECURONIUM BROMIDE	VECURONIUM BROMIDE
55150-235	VECURONIUM BROMIDE	VECURONIUM BROMIDE
55150-236	VECURONIUM BROMIDE	VECURONIUM BROMIDE
63323-781	Vecuronium Bromide	Vecuronium Bromide
63323-782	Vecuronium Bromide	Vecuronium Bromide
67457-438	VECURONIUM BROMIDE	VECURONIUM BROMIDE
67457-475	VECURONIUM BROMIDE	VECURONIUM BROMIDE
68083-139	Vecuronium Bromide	Vecuronium Bromide
68083-140	Vecuronium Bromide	Vecuronium Bromide
81565-206	Vecuronium Bromide	Vecuronium Bromide
25021-657	Vecuronium	vecuronium bromide
25021-658	Vecuronium	vecuronium bromide