NDC 60687-717
Diltiazem Hydrochloride 30 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-0318.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA074185
- On the market since
- Mar 27, 2023
- Package NDCs
60687-717-0160687-717-11- Official label
- DailyMed (National Library of Medicine), updated Sep 25, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?