Galantamine 70436-0005
Product NDC
70436-0005- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 2, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA077604
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Galantamine Hydrobromide | 8 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(1)
60 TABLET, FILM COATED in 1 BOTTLE (70436-005-06)