Strength
120 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335067513
Classification
Generic
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Last Updated
11/21/2018
Active Ingredients
DILTIAZEM HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA090492On Market Since
10/31/2011
Pharmacological Classes
Calcium Channel Antagonists
Calcium Channel Blocker
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