NDC 55154-4848
Lansoprazole 30 mg tablet, orally disintegrating, delayed release
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-3009.
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 USA, Inc. names for other drugs.
Recalls
- Mar 11, 2019 · Class III · Teva Pharmaceuticals USA
Subpotent Drug.
Lots: Lot #: 25Q002, Exp. 11/2019
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
- tablet, orally disintegrating, delayed release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA208784
- On the market since
- Mar 8, 2018
- Package NDCs
55154-4848-0- Official label
- DailyMed (National Library of Medicine), updated May 20, 2026
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