NDC 42291-030
Diltiazem Hydrochloride Extended-Release 120 mg capsule, extended release
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Mayne Pharma Inc.'s NDC 51862-330.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mayne Pharma International Pty Ltd. | Salisbury South, Australia | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 21, 2025 · 6 inspections |
| Catalent Greenville, Inc. | Greenville, NC, United States | Packages it and labels it | Problems found, fixed voluntarilyOct 24, 2025 · 13 inspections |
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- capsule, extended release
- Strength
- 120 mg
- Approval
- ANDA ANDA215775
- On the market since
- Jan 30, 2023
- Package NDCs
42291-030-01- Official label
- DailyMed (National Library of Medicine), updated Aug 29, 2023
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