NDC 17856-0087
Hydrocodone Polistirex and Chlorpheniramine Polistirexextended-release 8 mg per 5 mL / 10 mg per 5 mL suspension, extended release
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Cranbury Pharmaceuticals, LLC's NDC 27808-086.
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 Cranbury Pharmaceuticals, LLC names for other drugs.
Repackaging site
- Atlantic Biologicals Corps, Location not on file · repackages it
Recalls
- Jul 11, 2019 · Class II · Tris Pharma Inc.
Superpotent Drug and Failed Stability Specifications: High out-of-specification results for the active ingredients, hydrocodone and chlorpheniramine, as well as high out-of-specification results for the preservatives.
Lots: Lot#: 14079, Exp 10/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
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 ANDA091632
- On the market since
- Mar 6, 2015
- Package NDCs
17856-0087-117856-0087-217856-0087-3- Official label
- DailyMed (National Library of Medicine), updated Jan 10, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?