NDC 66220-719
Kristalose 10 g per 10 g powder, for solution
On the label: Cumberland 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 Cumberland Pharmaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Lactulose: every company that makes it
- Form
- powder, for solution, oral
- Strength
- 10 g per 10 g
- Approval
- ANDA ANDA074712
- On the market since
- Jan 20, 2012
- Package NDCs
66220-719-0166220-719-30- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2018
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