NDC 17856-0301
Hydrocodone Polistirex and Chlorpheniramine Polistirex 8 mg per 5 mL / 10 mg per 5 mL suspension, extended release
On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 62542-301, made by Neos Therapeutics LP (Hydrocodone Polistirex and Chlorpheniramine Polistirex). 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
- Chlorpheniramine and Hydrocodone: every company that makes it
- Form
- suspension, extended release
- Strength
- 8 mg per 5 mL / 10 mg per 5 mL
- Approval
- ANDA ANDA091671
- On the market since
- Oct 23, 2014
- Package NDCs
17856-0301-1- Official label
- DailyMed (National Library of Medicine), updated Jun 16, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?