NDC 17856-0067
Phenytoin 125 mg per 5 mL suspension
On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 60432-131, made by Morton Grove Pharmaceuticals, Inc. (Phenytoin). 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. 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 Atlantic Biologicals Corps. names for other drugs.
Product details
- Generic drug
- Phenytoin: every company that makes it
- Form
- suspension
- Strength
- 125 mg per 5 mL
- Approval
- ANDA ANDA040420
- On the market since
- Jun 24, 2002
- Package NDCs
17856-0067-3- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2009
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