NDC 71384-512
Dex-Moxi 1 mg per 1 mL / 5 mg per 1 mL injection, solution
On the label: Imprimis NJOF, LLC.
Where it's 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 Imprimis NJOF, LLC names for other drugs.
Recalls
- Dec 18, 2025 · Class II · Imprimis NJOF, LLC
Presence of particulate matter - Glass like particles.
Lots: Lot: 25MAY051, Expires: 06/26/2026; 25AUG003, Expires:08/07/2026 - May 14, 2024 · Class II · Imprimis NJOF, LLC
Lack of Assurance of Sterility
Lots: Lot #: 23MAY016, Exp. Date 5/8/24; 23JUL016, Exp. Date 7/10/24; 23AUG034, Exp. Date 8/16/24; 23DEC014, Exp. Date 12/10/24
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dexamethasone and Moxifloxacin: every company that makes it
- Form
- injection, solution
- Strength
- 1 mg per 1 mL / 5 mg per 1 mL
- Approval
- unapproved drug other
- On the market since
- Jan 5, 2018
- Package NDCs
71384-512-01- Official label
- DailyMed (National Library of Medicine), updated Feb 10, 2020
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