Galantamine 68084-0729
Product NDC
68084-0729- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 3, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA090957
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Galantamine Hydrobromide | 4 mg/1 |
Drug Class
Cholinesterase Inhibitor [EPC]Cholinesterase Inhibitors [MoA]
Packaging Options(1)
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-729-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-729-11)