Famotidine 00641-6022
Product NDC
00641-6022- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 16, 2001
- Listing Expires
- December 31, 2026
- Application
- ANDA075486
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Famotidine | 10 mg/mL |
Drug Class
Histamine-2 Receptor Antagonist [EPC]Histamine H2 Receptor Antagonists [MoA]Histamine-2 Receptor Antagonist [EPC]
Packaging Options(1)
25 VIAL in 1 CARTON (0641-6022-25) / 2 mL in 1 VIAL (0641-6022-01)