NDC 53808-0200
Amlodipine Besylate 5 mg tablet
On the label: State of Florida DOH Central Pharmacy.
It's a repackaged product (source NDC 31722-0238, which isn't on a current label).
Where it's 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 State of Florida DOH Central Pharmacy uses for other drugs.
Product details
- Generic drug
- Amlodipine: see every company that makes it
- Form
- tablet
- Strength
- 5 mg
- Approval
- ANDA ANDA077955
- On the market since
- Jul 1, 2009
- Package NDCs
53808-0200-1- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?