NDC 43598-012
Augmentin 125 mg per 5 mL / 31.25 mg per 5 mL powder, for suspension
On the label: Dr. Reddy's Laboratories Inc..
Where it's 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 |
Product details
- Generic drug
- Amoxicillin and Clavulanic Acid: every company that makes it
- Form
- powder, for suspension
- Strength
- 125 mg per 5 mL / 31.25 mg per 5 mL
- Approval
- NDA NDA050575
- On the market since
- Oct 22, 1990
- Package NDCs
43598-012-5143598-012-5243598-012-53- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2016
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