NDC 81033-023
Famotidine 40 mg per 5 mL powder, for suspension
On the label: Kesin Pharma Corporation.
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 Kesin Pharma Corporation names for other drugs.
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 40 mg per 5 mL
- Approval
- ANDA ANDA217137
- On the market since
- Aug 10, 2023
- Package NDCs
81033-023-50- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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