NDC 70332-109
Ranitidine Hydrochloride Oral Suspension Kit 6.4 g per 6.4 g kit
On the label: Fusion Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| California Pharmaceuticals LLC | Camarillo, California, United States | Makes it and repackages it | Problems found, fixed voluntarilyDec 12, 2018 · 6 inspections |
Product details
- Generic drug
- Ranitidine: every company that makes it
- Form
- kit
- Strength
- 6.4 g per 6.4 g
- Approval
- unapproved drug other
- On the market since
- Jan 2, 2017
- Package NDCs
70332-109-01- Official label
- DailyMed (National Library of Medicine), updated Jan 5, 2018
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