NDC 70518-4275
Admelog 100 U per 1 mL injection, solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Sanofi-Aventis U.S. LLC's NDC 0024-5925.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sanofi-Aventis Deutschland GmbH | Frankfurt am Main, Germany | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 25, 2022 · 10 inspections, 1 with FDA action |
Recalls
- Apr 11, 2023 · Class II · Sanofi-Aventis U.S. LLC
Lack of Assurance of Sterility: Malformed crimped collar seal
Lots: Lot # 3F497B, EXP 12-31-2025 - Jul 5, 2018 · Class II · Sanofi-Aventis U.S. LLC
Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.
Lots: Lot #: 7F021B, Exp 6/30/20
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 Lispro: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 100 U per 1 mL
- Approval
- BLA BLA209196
- On the market since
- Feb 4, 2025
- Package NDCs
70518-4275-0- Official label
- DailyMed (National Library of Medicine), updated Sep 3, 2026
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