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
- Nov 2, 2018 · Class II · Sandoz Inc
Cross Contamination with Other Products
Lots: Lots: a) JA9535 Exp. 05/2021.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Isosorbide Dinitrate: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA089367
- On the market since
- Jan 7, 1988
- Package NDCs
0781-1695-010781-1695-100781-1695-13- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?