NDC 0480-4138

Lubiprostone 24 ug capsule, gelatin coated

On the label: Teva 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 Teva Pharmaceuticals, Inc. names for other drugs.

Product details

Generic drug
Lubiprostone: every company that makes it
Form
capsule, gelatin coated, oral
Strength
24 ug
Approval
ANDA ANDA209920
On the market since
Jan 3, 2023
Package NDCs
0480-4138-06
Official label
DailyMed (National Library of Medicine), updated May 27, 2022

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