Insulin Diluting Medium for NovoLog 1 mL per 1 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 Novo Nordisk names for other drugs.

Recalls

• Mar 22, 2021 · Class I · Novo Nordisk Inc
  Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
  Lots: KS6BS11, Exp 11/30/2021
• Mar 22, 2021 · Class I · Novo Nordisk Inc
  Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
  Lots: JZFC826 exp 06/30/2021; KZFM305 exp 08/31/2022

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

Product details

Generic drug

Water: every company that makes it

Form

injection, solution, intravenous; subcutaneous

Strength

1 mL per 1 mL

Approval

BLA BLA020986

On the market since

Aug 27, 2001

Package NDCs

0169-2001-90

Official label

DailyMed (National Library of Medicine), updated Feb 28, 2023

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