Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| California Pharmaceuticals LLC | Camarillo, California, United States | Makes it | Problems found, fixed voluntarilyDec 12, 2018 · 6 inspections |
Recalls
- Mar 6, 2015 · Class II · Fusion Pharmaceuticals, LLC
Microbial Contamination of a Non-Sterile Product: Kit component is contaminated with Burkholderia multivorans.
Lots: Lot Numbers: PL713, PL714, PL715, PL716, PL717, PL718, PL719, PL720, PL721, PL722, PL735, PL736, PL737, PL738, PL739, PL740, PL741, PL742, PL743, PL744; Expiry: 7/20/2015.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Diphenhydramine: every company that makes it
- Form
- kit
- Strength
- 0.75 g per 0.75 g
- Approval
- unapproved drug other
- On the market since
- Feb 8, 2010
- Package NDCs
43093-104-01- Official label
- DailyMed (National Library of Medicine), updated Nov 19, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?