NDC 53002-2101
Sulfamethoxazole and Trimethoprim 160 mg / 800 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-233.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Sulfamethoxazole and Trimethoprim: every company that makes it
- Form
- tablet
- Strength
- 160 mg / 800 mg
- Approval
- ANDA ANDA090624
- On the market since
- Feb 16, 2010
- Package NDCs
53002-2101-153002-2101-253002-2101-353002-2101-453002-2101-5- Official label
- DailyMed (National Library of Medicine), updated Dec 15, 2020
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