NDC 0591-2990
Fluocinolone Acetonide Topical 0.1 mg per 1 mL solution
On the label: Actavis Pharma, Inc..
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 Actavis Pharma, Inc. names for other drugs.
Recalls
- Jul 5, 2018 · Class II · Teva Pharmaceuticals USA
Failed Impurities and Degradation Specifications and Subpotent Drug: out-of-specification (OOS) test results for below assay and above specification for degradants.
Lots: Lot #s: 1164898, EXP 10/18; 1164904, 1164909, EXP 11/18; 1211396, EXP 07/19; 1230808, 1231127, EXP 01/20
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluocinolone Acetonide: every company that makes it
- Form
- solution, topical
- Strength
- 0.1 mg per 1 mL
- Approval
- ANDA ANDA208386
- On the market since
- Dec 7, 2016
- Package NDCs
0591-2990-60- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2016
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