Galantamine
- Product NDC
- 0615-7542
- 11-digit product format
- 006157542
- Labeler code
- 0615
- Product ID
- 0615-7542_a2a1a050-21be-46bd-954f-0a97017e9d38
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077590
- Marketing category
- ANDA
- Marketing start
- 2009-05-29
- Marketing end
- 0000-00-00
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record