Famotidine 51655-0233
Product NDC
51655-0233- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 17, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA075511
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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(3)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-25)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-26)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-52)