Zoledronic Acid 5 mg per 100 mL injection, solution

Where it's 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 Dr. Reddy's Laboratories Inc. names for other drugs.

Recalls

• Sep 12, 2018 · Class III · Dr. Reddy's Laboratories, Inc.
  Failed Impurities/Degradation Specifications: OOS for unknown impurities.
  Lots: Batch Numbers: BS704, EXP 12/018; BS725, EXP 6/2019; BS745, EXP 11/2019.

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Zoledronic Acid: every company that makes it

Form

injection, solution, intravenous

Strength

5 mg per 100 mL

Approval

ANDA ANDA091363

On the market since

Aug 19, 2013

Package NDCs

43598-331-11

Official label

DailyMed (National Library of Medicine), updated Jul 20, 2017

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