NDC 0713-0222
Fluocinolone Acetonide 0.25 mg per 1 g cream
On the label: Cosette Pharmaceuticals, 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 Cosette Pharmaceuticals, Inc. names for other drugs.
Recalls
- Sep 30, 2013 · Class III · G & W Laboratories Inc
Failed Content Uniformity Specifications; at the 18 month time point.
Lots: 15 gm Lot #: 022211002, 022212001- 022212008, 022212010-022212012, 022212017, 022213001, 022213005, 022213008 60 gm Lot #: 022211002, 022212001- 022212007, 022212009, 022212010, 022212012-022212016, 022212018, 022212019, 022213002.
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
- cream
- Strength
- 0.25 mg per 1 g
- Approval
- ANDA ANDA089525
- On the market since
- Jul 26, 1988
- Package NDCs
0713-0222-150713-0222-60- Official label
- DailyMed (National Library of Medicine), updated Nov 22, 2023
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