NDC 50436-0129

Bumetanide 1 mg tablet

On the label: Unit Dose Services. It's a repackaged product: Unit Dose Services 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 aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sandoz Inc. uses for other drugs.

Repackaging site

• Unit Dose Services, · repackages it and relabels it

Recalls

• Nov 6, 2013 · Class III · Terminated
  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

Product details

Generic drug

Bumetanide: see every company that makes it

Form

tablet

Strength

1 mg

Approval

ANDA ANDA074700

On the market since

Nov 21, 1996

Package NDCs

50436-0129-1

Official label

DailyMed (National Library of Medicine), updated Apr 3, 2018

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?