NDC 42708-104
Pantoprazole Sodium 40 mg tablet, delayed release
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-713.
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 Camber Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Mar 26, 2026 · Class II · Hetero Labs Limited (Unit V)
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
Lots: Batch # FD253967, Exp Date: 06/26/2027 - Mar 14, 2023 · Class II · Hetero USA Inc
CGMP Deviations: Discoloration
Lots: Lot #: PAN22542, Exp. Date: 9/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA202882
- On the market since
- Sep 10, 2014
- Package NDCs
42708-104-30- Official label
- DailyMed (National Library of Medicine), updated Dec 4, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?