NDC 70166-536
Phenobarbital 20 mg per 5 mL liquid
On the label: Lohxa. It's repackaged from NDC 16571-330, made by Rising Pharmaceuticals, Inc. (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 Lohxa names for other drugs.
Recalls
- Mar 25, 2019 · Class II · Lohxa LLC
Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.
Lots: Lot# M12031, Exp. 12/2019; T01241 Exp. 02/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Phenobarbital: every company that makes it
- Form
- liquid
- Strength
- 20 mg per 5 mL
- Approval
- unapproved drug other
- On the market since
- Feb 13, 2018
- Package NDCs
70166-536-02- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2018
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?