NDC 70518-4187
Betamethasone Dipropionate 0.5 mg per 1 g cream
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from E. FOUGERA & CO., A division of Nycomed US Inc.'s NDC 0168-0055.
Where the pills inside were 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.
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Betamethasone: every company that makes it
- Form
- cream, topical
- Strength
- 0.5 mg per 1 g
- Approval
- NDA NDA019137
- On the market since
- Sep 26, 2024
- Package NDCs
70518-4187-0- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?