Famotidine 72789-0331
Product NDC
72789-0331- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 4, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA215767
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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(6)
2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-02)
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-20)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-30)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-60)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-90)
180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-93)