Famotidine 72865-0214
Product NDC
72865-0214- Manufacturer
- Xlcare Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 15, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA215689
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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 (72865-214-01)
500 TABLET, FILM COATED in 1 BOTTLE (72865-214-05)
180 TABLET, FILM COATED in 1 BOTTLE (72865-214-18)
30 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)