NDC 50436-0712

Pantoprazole Sodium 20 mg tablet, delayed release

On the label: Unit Dose Services. It's a repackaged product: Unit Dose Services rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-712.

Where the pills inside were made

This label doesn't name the factory that makes the drug. Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Camber Pharmaceuticals Inc. uses for other drugs.

Repackaging site

• Unit Dose Services, · repackages it and relabels it

Recalls

• Mar 26, 2026 · Class II · Ongoing
  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 · Ongoing
  CGMP Deviations: Discoloration
  Lots: Lot #: PAN22542, Exp. Date: 9/2024

Product details

Generic drug

Pantoprazole: see every company that makes it

Form

tablet, delayed release

Strength

20 mg

Approval

ANDA ANDA202882

On the market since

Sep 10, 2014

Package NDCs

50436-0712-2

Official label

DailyMed (National Library of Medicine), updated Aug 24, 2021

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