NDC 51662-1200
Activated Charcoal 208 mg per 1 mL suspension
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged from NDC 0574-0121, made by Padagis US LLC (Actidose Aqua). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants HF Acquisition Co. LLC. DBA HealthFirst names for other drugs.
Product details
- Generic drug
- Activated Charcoal: every company that makes it
- Form
- suspension
- Strength
- 208 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- Dec 22, 2018
- Package NDCs
51662-1200-1- Official label
- DailyMed (National Library of Medicine), updated Feb 19, 2020
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