NDC 53808-0695
Diltiazem HydrochlorideExtended Release 240 mg capsule, coated, extended release
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 49884-831, made by Par Pharmaceutical, Inc. (Diltiazem HydrochlorideExtended Release). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- capsule, coated, extended release
- Strength
- 240 mg
- Approval
- ANDA ANDA074984
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0695-2- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?