Famotidine 68071-3420
Product NDC
68071-3420- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 8, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA215630
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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(5)
30 TABLET, FILM COATED in 1 BOTTLE (68071-3420-3)
60 TABLET, FILM COATED in 1 BOTTLE (68071-3420-6)
14 TABLET, FILM COATED in 1 BOTTLE (68071-3420-7)
120 TABLET, FILM COATED in 1 BOTTLE (68071-3420-8)
90 TABLET, FILM COATED in 1 BOTTLE (68071-3420-9)