NDC 53808-0798
Sulfamethoxazole and Trimethoprim 160 mg / 800 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Amneal Pharmaceuticals's NDC 53746-272.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Amneal Pharmaceuticals names for other drugs.
Recalls
- Sep 27, 2011 · Class II · Shamrock Medical Solutions Group LLC
Labeling: Label Mix up; product labeled to contain Sulfamethoxazole and Trimethoprim Tablets, 400 mg/80 mg instead of Sulfamethoxazole and Trimethoprim Tablets, 800 mg/160 mg
Lots: Lot 00288N, Use By: 9/15/2012, NDC 53746-272-01
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sulfamethoxazole and Trimethoprim: every company that makes it
- Form
- tablet
- Strength
- 160 mg / 800 mg
- Approval
- ANDA ANDA076899
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0798-1- Official label
- DailyMed (National Library of Medicine), updated Aug 19, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?