Neostigmine

Product NDC
71872-7178
11-digit product format
718727178
Labeler code
71872
Product ID
71872-7178_fbbd062c-6f20-ac06-e053-6394a90a529f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Neostigmine
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Medical Purchasing Solutions, LLC
Application
ANDA209135
Marketing category
ANDA
Marketing start
2018-09-04
Substance
NEOSTIGMINE METHYLSULFATE
Active strength
1 mg/mL
Pharmacologic classes
Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
98IMH7M386NEOSTIGMINE METHYLSULFATE51-60-5NEOSTIGMINE METHYLSULFATE
3982TWQ96GNEOSTIGMINE59-99-4Neostigmine

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71872-7178-1718727178011 VIAL, MULTI-DOSE in 1 BAG (71872-7178-1) / 10 mL in 1 VIAL, MULTI-DOSE2019-09-12NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NeostigmineMedical Purchasing Solutions, LLC2023-05-15HUMAN PRESCRIPTION DRUG LABEL2