Strength
30 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093031801
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
DILTIAZEM HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA074185On Market Since
12/22/1995
Pharmacological Classes
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