NDC 42254-282
Amoxicillin and Clavulanate Potassium 57 mg per 5 mL / 400 mg per 5 mL powder, for suspension
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-208.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Beecham Pharmaceuticals (PTE) Limited | Location not on file | Makes the active ingredient and tests it | Not inspected on record |
| Dr. Reddy's Laboratories Inc DBA Dr. Reddy's Laboratories Tennessee LLC | Location not on file | Makes it | Not inspected on record |
| SmithKline Beecham Limited | Worthing, United Kingdom | Makes the active ingredient and tests it | Serious problems, FDA actionJul 10, 2015 · 3 inspections, 2 with FDA action |
Repackaging site
- Dispensing Solutions Inc., Santa Ana, California, United States · repackages it and relabels it
- Keltman Pharmaceuticals Inc., Location not on file · repackages it
- PSS World Medical, Inc., Olathe, Kansas, United States · repackages it
- Rebel Distributors Corp., Location not on file · repackages it and relabels it
- Script Pak, Location not on file · repackages it and relabels it
- Stat Rx USA, Location not on file · repackages it
Product details
- Generic drug
- Amoxicillin and Clavulanic Acid: every company that makes it
- Form
- powder, for suspension
- Strength
- 57 mg per 5 mL / 400 mg per 5 mL
- Approval
- NDA NDA050575
- On the market since
- Oct 22, 1990
- Package NDCs
42254-282-00- Official label
- DailyMed (National Library of Medicine), updated Aug 28, 2012
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