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Neostigmine Methylsulfate - 0641-6140-10 - (Neostigmine Methylsulfate)

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Drug Information of Neostigmine Methylsulfate

Product NDC: 0641-6140
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
Coding System: National Drug Codes(NDC)

Labeler Information of Neostigmine Methylsulfate

Product NDC: 0641-6140
Labeler Name: West-ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19730101

Package Information of Neostigmine Methylsulfate

Package NDC: 0641-6140-10
Package Description: 10 VIAL in 1 CARTON (0641-6140-10) > 10 mL in 1 VIAL (0641-6140-01)

NDC Information of Neostigmine Methylsulfate

NDC Code 0641-6140-10
Proprietary Name Neostigmine Methylsulfate
Package Description 10 VIAL in 1 CARTON (0641-6140-10) > 10 mL in 1 VIAL (0641-6140-01)
Product NDC 0641-6140
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Neostigmine Methylsulfate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19730101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name West-ward Pharmaceutical Corp.
Substance Name NEOSTIGMINE METHYLSULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Neostigmine Methylsulfate


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