NDC 51662-1314
Vasopressin 20 [USP'U] 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 ENDO USA, Inc.'s NDC 42023-164.
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 ENDO USA, Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Jan 11, 2024 · Class II · Par Sterile Products LLC
Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.
Lots: Lot # 66702; Exp. 02/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Vasopressin, Unspecified: every company that makes it
- Form
- injection, intravenous
- Strength
- 20 [USP'U] per 1 mL
- Approval
- NDA NDA204485
- On the market since
- Nov 17, 2018
- Package NDCs
51662-1314-151662-1314-2- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2021
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