NDC 53808-0626
Isosorbide Dinitrate 20 mg tablet
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from Sandoz Inc.'s NDC 0781-1695.
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.
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
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
- Strength
- 20 mg
- Approval
- ANDA ANDA089367
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0626-2- Official label
- DailyMed (National Library of Medicine), updated Sep 12, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?