Strength
300 mg/1
Manufacturer
Oceanside PharmaceuticalsNDC
68682099898
Classification
Generic
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Last Updated
9/17/2025
Active Ingredients
DILTIAZEM HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA075116On Market Since
12/28/1999
Pharmacological Classes
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