Neostigmine

Product NDC
43598-529
11-digit product format
435980529
Labeler code
43598
Product ID
43598-529_649d8760-81df-13da-6556-14a0fdbc8b02
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Neostigmine
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Dr.Reddy's Laboratories Inc
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
43598-529-11435980529111 VIAL, MULTI-DOSE in 1 CARTON (43598-529-11) / 10 mL in 1 VIAL, MULTI-DOSE2018-09-04NoNoHistorical
43598-529-364359805293610 VIAL, MULTI-DOSE in 1 CARTON (43598-529-36) / 10 mL in 1 VIAL, MULTI-DOSE2018-09-04NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NeostigmineMedical Purchasing Solutions, LLC2023-05-15HUMAN PRESCRIPTION DRUG LABEL2
NeostigmineDr.Reddy's Laboratories Inc | Gland Pharma Ltd2021-02-02HUMAN PRESCRIPTION DRUG LABEL4