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Neostigmine Methylsulfate - 63323-383-10 - (NEOSTIGMINE METHYLSULFATE)

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Drug Information of Neostigmine Methylsulfate

Product NDC: 63323-383
Proprietary Name: Neostigmine Methylsulfate
Non Proprietary Name: NEOSTIGMINE METHYLSULFATE
Active Ingredient(s): 1    mg/mL & nbsp;   NEOSTIGMINE METHYLSULFATE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Neostigmine Methylsulfate

Product NDC: 63323-383
Labeler Name: Fresenius Kabi USA, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000901

Package Information of Neostigmine Methylsulfate

Package NDC: 63323-383-10
Package Description: 10 VIAL, MULTI-DOSE in 1 TRAY (63323-383-10) > 10 mL in 1 VIAL, MULTI-DOSE

NDC Information of Neostigmine Methylsulfate

NDC Code 63323-383-10
Proprietary Name Neostigmine Methylsulfate
Package Description 10 VIAL, MULTI-DOSE in 1 TRAY (63323-383-10) > 10 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-383
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NEOSTIGMINE METHYLSULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20000901
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Fresenius Kabi USA, LLC
Substance Name NEOSTIGMINE METHYLSULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Neostigmine Methylsulfate


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