NDC 68788-4141
Lansoprazole 30 mg capsule, delayed release pellets
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-8030.
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 Mylan Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Recalls
- Jan 30, 2013 · Class II · Mylan Pharmaceuticals Inc.
Presence of Foreign Tablets/Capsules: Bottles of lansoprazole 30 mg delayed-release capsules may contain topiramate 100 mg tablets.
Lots: Lot #: 1110829, Exp 05/14
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lansoprazole: every company that makes it
- Form
- capsule, delayed release pellets, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA090763
- On the market since
- Aug 12, 2026
- Package NDCs
68788-4141-368788-4141-668788-4141-9- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2026
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