NDC 51662-1527
Atropine Sulfate 0.1 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 International Medication Systems, Ltd.'s NDC 76329-3340.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| International Medication Systems, Ltd. | South El Monte, CA, United States | Makes it, makes the active ingredient and tests it | Serious problems, FDA actionDec 19, 2025 · 15 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Atropine: every company that makes it
- Form
- injection, intravenous
- Strength
- 0.1 mg per 1 mL
- Approval
- ANDA ANDA212461
- On the market since
- Apr 25, 2021
- Package NDCs
51662-1527-151662-1527-251662-1527-3- Official label
- DailyMed (National Library of Medicine), updated Jan 22, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?