NDC 82804-304

Lubiprostone 24 ug capsule, gelatin coated

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Teva Pharmaceuticals, Inc.'s NDC 0480-4138.

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 Teva Pharmaceuticals, Inc. names for other drugs.

Repackaging site

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
82804-304-60
Official label
DailyMed (National Library of Medicine), updated Jul 1, 2026

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?