Famotidine 68788-8889
Product NDC
68788-8889- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 23, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA075718
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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(4)
100 TABLET, FILM COATED in 1 BOTTLE (68788-8889-1)
30 TABLET, FILM COATED in 1 BOTTLE (68788-8889-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-8889-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-8889-9)