NDC 76420-835
epinephrine 0.15 mg per 0.15 mL injection
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Amneal Pharmaceuticals's NDC 0115-1695.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Boehringer Ingelheim Pharma GmbH and Co. KG | Ingelheim am Rhein, Germany | Makes the active ingredient | Problems found, fixed voluntarilyMay 15, 2025 · 8 inspections, 1 with FDA action |
| Hospira, Inc. | McPherson, KS, United States | Makes it and tests it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
| PPD Development, L.P. | Middleton, WI, United States | Tests it | Problems found, fixed voluntarilySep 25, 2025 · 6 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Product details
- Generic drug
- Epinephrine: every company that makes it
- Form
- injection, subcutaneous
- Strength
- 0.15 mg per 0.15 mL
- Approval
- NDA authorized generic NDA020800
- On the market since
- Apr 1, 2010
- Package NDCs
76420-835-0176420-835-02- Official label
- DailyMed (National Library of Medicine), updated Aug 2, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?