NDC 68462-608
Clobetasol Propionate 0.5 mg per 1 g aerosol, foam
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Chhatrapati Sambhajinagar (previously known as Aurangabad), India | Makes it and tests it | No problems foundSep 20, 2024 · 5 inspections |
Recalls
- Nov 15, 2019 · Class III · Glenmark Pharmaceuticals Inc., USA
Defective delivery system; product is not foaming or is coming out as liquid.
Lots: a) 14190026, 14190028, 14190029, exp Feb-2021, 14190043, 14190045 exp Apr-2021 b) 14190024, 14190025, 14190027, exp Feb-2021, 14190030, 14190031, exp Mar-2021, 14190039, 14190042 exp Apr-2021, 14190047 exp May-2021, 14190062 exp Jul-2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Clobetasol: every company that makes it
- Form
- aerosol, foam, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA210809
- On the market since
- Feb 16, 2019
- Package NDCs
68462-608-2768462-608-94- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2026
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