Neostigmine Methylsulfate
- Product NDC
- 52584-415
- 11-digit product format
- 525840415
- Labeler code
- 52584
- Product ID
- 52584-415_740b0130-1a54-4e0b-820e-f7da204d5eeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neostigmine Methylsulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc
- Application
- NDA203629
- Marketing category
- NDA
- Marketing start
- 2016-08-11
- Marketing end
- 0000-00-00
- Substance
- NEOSTIGMINE METHYLSULFATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record