NDC 21695-338
Ranitidine Hydrochloride 300 mg capsule
On the label: Rebel Distributors Corp... It's repackaged: Rebel Distributors Corp.. rebottles it from Sandoz Inc.'s NDC 0781-2865.
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 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: HD8625 4/30/2020 HD9275 4/30/2020 HU2207 8/31/2020 HX6676 3/31/2021 HX6677 3/31/2021
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
- 300 mg
- Approval
- ANDA ANDA074655
- On the market since
- Oct 22, 1997
- Package NDCs
21695-338-30- 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?