NDC 17856-1508
Phenobarbital 20.0 mg per 5 mL elixir
On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 0603-1508, made by Par Pharmaceutical (Phenobarbital). 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 repackages it and 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 Atlantic Biologicals Corps. names for other drugs.
Product details
- Generic drug
- Phenobarbital: every company that makes it
- Form
- elixir
- Strength
- 20.0 mg per 5 mL
- Approval
- UNAPPROVED DRUG OTHER
- On the market since
- Jan 1, 1997
- Package NDCs
17856-1508-117856-1508-217856-1508-5- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?