NDC 51662-1619
Atropine Sulfate 0.4 mg per 1 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0641-6251.
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 Hikma Pharmaceuticals USA Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Atropine: every company that makes it
- Form
- injection, endotracheal; intramedullary; intramuscular; intravenous; subcutaneous
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA213561
- On the market since
- Oct 1, 2022
- Package NDCs
51662-1619-151662-1619-251662-1619-3- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2024
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