Galantamine
- Product NDC
- 0378-2721
- 11-digit product format
- 003782721
- Labeler code
- 0378
- Product ID
- 0378-2721_8ef24417-c577-412c-80fe-06a747cbd70f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA077590
- Marketing category
- ANDA
- Marketing start
- 2008-08-29
- Marketing end
- 2019-12-31
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record