Ranitidine Hydrochloride 150 mg capsule

Where it's 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 Sandoz Inc. names for other drugs.

Recalls

• Sep 23, 2019 · Class II · Sandoz, Inc
  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 · Sandoz, Inc
  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

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Ranitidine: every company that makes it

Form

capsule

Strength

150 mg

Approval

ANDA ANDA074655

On the market since

Oct 22, 1997

Package NDCs

0781-2855-05 0781-2855-31 0781-2855-60 0781-2855-92

Official label

DailyMed (National Library of Medicine), updated Aug 18, 2020

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