NDC 51662-1429
Methylprednisolone Acetate 40 mg per 1 mL injection, suspension
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged from NDC 0703-0031, made by Teva Parenteral Medicines, Inc. (Methylprednisolone Acetate). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). 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 HF Acquisition Co. LLC. DBA HealthFirst names for other drugs.
Product details
- Generic drug
- Methylprednisolone: every company that makes it
- Form
- injection, suspension
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA040557
- On the market since
- Dec 21, 2019
- Package NDCs
51662-1429-1- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2020
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