Famotidine 68071-2306
Product NDC
68071-2306- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 16, 2001
- Listing Expires
- December 31, 2026
- Application
- ANDA075805
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Famotidine | 20 mg/1 |
Drug Class
Histamine-2 Receptor Antagonist [EPC]Histamine H2 Receptor Antagonists [MoA]Histamine-2 Receptor Antagonist [EPC]
Packaging Options(2)
30 TABLET in 1 BOTTLE (68071-2306-3)
180 TABLET in 1 BOTTLE (68071-2306-8)