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Neostigmine methylsulfate

These highlights do not include all the information needed to use NEOSTIGMINE METHYLSULFATE INJECTION safely and effectively. See full prescribing information for NEOSTIGMINE METHYLSULFATE INJECTION.  NEOSTIGMINE METHYLSULFATE Injection, for intravenous use  Initial U.S. Approval: 1939

Approved
Approval ID

971713db-d5ac-44c1-ada5-a56a943d79bf

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 18, 2022

Manufacturers
FDA

BE Pharmaceuticals Inc.

DUNS: 081499296

Products 2

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Neostigmine methylsulfate

PRODUCT DETAILS

NDC Product Code71839-106
Application NumberANDA212512
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateMarch 17, 2022
Generic NameNeostigmine methylsulfate

INGREDIENTS (6)

PHENOLInactive
Quantity: 4.5 mg in 1 mL
Code: 339NCG44TV
Classification: IACT
NEOSTIGMINE METHYLSULFATEActive
Quantity: 1 mg in 1 mL
Code: 98IMH7M386
Classification: ACTIB
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: IACT
SODIUM ACETATEInactive
Quantity: 0.2 mg in 1 mL
Code: 4550K0SC9B
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT

Neostigmine methylsulfate

PRODUCT DETAILS

NDC Product Code71839-105
Application NumberANDA212512
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateMarch 17, 2022
Generic NameNeostigmine methylsulfate

INGREDIENTS (6)

NEOSTIGMINE METHYLSULFATEActive
Quantity: 0.5 mg in 1 mL
Code: 98IMH7M386
Classification: ACTIB
SODIUM ACETATEInactive
Quantity: 0.2 mg in 1 mL
Code: 4550K0SC9B
Classification: IACT
PHENOLInactive
Quantity: 4.5 mg in 1 mL
Code: 339NCG44TV
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
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Neostigmine methylsulfate - FDA Approval | MedPath