NDC 50090-3491
Tresiba 200 U per 1 mL injection, solution
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Novo Nordisk's NDC 0169-2550.
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 Novo Nordisk names for other drugs.
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
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: JP52771 exp 09/30/2021; JP53136 exp 06/30/2021; KP50575 exp 01/31/2022; KP50976 exp 01/31/2022; KP51813 exp 04/30/2022; KP52035 exp 04/30/2022; KP52117 exp 04/30/2022; KP52440 exp 06/30/2022; KP52461 exp 04/30/2022; KP52616 exp 06/30/2022; JP52361 exp 08/01/2021 - 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: JZFE233 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: KP52829 exp 07/31/2022; JP54181 exp 09/30/2021; KP51059 exp 11/30/2021; KP51865 exp 11/30/2021; KP54179 exp 11/30/2022; JP52179 exp 08/16/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Insulin Degludec: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 200 U per 1 mL
- Approval
- BLA BLA203314
- On the market since
- Sep 25, 2015
- Package NDCs
50090-3491-0- Official label
- DailyMed (National Library of Medicine), updated Dec 12, 2023
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