NDC 69097-992
Diltiazem Hydrochloride 120 mg tablet, extended release
On the label: Cipla USA., Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 120 mg
- Approval
- ANDA ANDA216327
- On the market since
- Jun 12, 2023
- Package NDCs
69097-992-0269097-992-05- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?