NDC 68387-381
Doxycycline 100 mg tablet, coated
On the label: Keltman Pharmaceuticals Inc.. It's repackaged: Keltman Pharmaceuticals Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-2112.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Recalls
- May 13, 2020 · Class II · West-Ward Columbus Inc
Failed dissolution specification: The dissolution test at the 24 month time point (end of shelf life) yielded an out of specification result.
Lots: Lot #: a) 71846B, Exp 6/2021; b) 71726A, Exp 6/2020; 71846B, 71853A, Exp 6/2021 - Jul 24, 2018 · Class II · West-Ward Columbus Inc
Failed Dissolution Specifications:
Lots: Lot# 71545B, Expiry date: 01/19 - Jul 24, 2018 · Class II · West-Ward Columbus Inc
Failed Dissolution Specifications:
Lots: Lot# 71545A, Expiry date: 07/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Doxycycline: every company that makes it
- Form
- tablet, coated
- Strength
- 100 mg
- Approval
- ANDA ANDA065095
- On the market since
- Jan 10, 2011
- Package NDCs
68387-381-20- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2011
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