NDC 0168-0268
Betamethasone Dipropionate 0.5 mg per 1 g ointment, augmented
On the label: E. FOUGERA & CO., A division of Nycomed US 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 E. FOUGERA & CO., A division of Nycomed US Inc. names for other drugs.
Product details
- Generic drug
- Betamethasone: every company that makes it
- Form
- ointment, augmented, topical
- Strength
- 0.5 mg per 1 g
- Approval
- ANDA ANDA075373
- On the market since
- Jun 22, 1999
- Package NDCs
0168-0268-150168-0268-50- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2026
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