NDC 21695-337

Ranitidine Hydrochloride 150 mg capsule

On the label: Rebel Distributors Corp... It's a repackaged product: Rebel Distributors Corp.. rebottles it from Sandoz Inc.'s NDC 0781-2855.

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 Sandoz Inc. uses for other drugs.

Recalls

• Sep 23, 2019 · Class II · Terminated
  CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
  Lots: HC9266 4/30/2020 HD1865 4/30/2020 HP9441 9/30/2020 JK7994 8/31/2021 JK8659 8/31/2021
• Sep 23, 2019 · Class II · Terminated
  CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
  Lots: HD1862 4/30/2020 HP9438 9/30/2020 HP9439 9/30/2020 HP9440 9/30/2020

Product details

Generic drug

Ranitidine: see every company that makes it

Form

capsule

Strength

150 mg

Approval

ANDA ANDA074655

On the market since

Oct 22, 1997

Package NDCs

21695-337-60

Official label

DailyMed (National Library of Medicine), updated Nov 11, 2010

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