NDC 82804-119
Bumetanide 1 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Sandoz Inc.'s NDC 0185-0129.
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 Sandoz Inc. names for other drugs.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Nov 6, 2013 · Class III · Sandoz Inc
Failed Moisture Limit; Out of Specification (OOS) results were obtained for moisture content during stability testing at the 12 month time point, controlled room temperature conditions.
Lots: Lot #: a) CU6131, b) CW1161
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Bumetanide: every company that makes it
- Form
- tablet, oral
- Strength
- 1 mg
- Approval
- ANDA ANDA074700
- On the market since
- Nov 21, 1996
- Package NDCs
82804-119-90- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?