NDC 70518-2283
Epinephrine 0.3 mg per 0.3 mL injection
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-5986.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 033J20AA - Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 025C20AA - Mar 5, 2020 · Class II · Teva Pharmaceuticals USA
CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.
Lots: Lot # 007F19AA, exp. date 04/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Epinephrine: every company that makes it
- Form
- injection, intramuscular; subcutaneous
- Strength
- 0.3 mg per 0.3 mL
- Approval
- ANDA ANDA090589
- On the market since
- Aug 26, 2019
- Package NDCs
70518-2283-0- Official label
- DailyMed (National Library of Medicine), updated Feb 3, 2026
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