Product Details for ANDA 074852
DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
120MG
Marketing Status: Discontinued
180MG
Marketing Status: Discontinued
240MG
Marketing Status: Discontinued
120MG
Marketing Status: Discontinued
Active Ingredient: DILTIAZEM HYDROCHLORIDE
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 120MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074852
Product Number: 001
Approval Date: Oct 10, 1997
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 120MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074852
Product Number: 001
Approval Date: Oct 10, 1997
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
180MG
Marketing Status: Discontinued
Active Ingredient: DILTIAZEM HYDROCHLORIDE
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 180MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074852
Product Number: 002
Approval Date: Oct 10, 1997
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
DILTIAZEM HYDROCHLORIDE (DILTIAZEM HYDROCHLORIDE)
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 180MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074852
Product Number: 002
Approval Date: Oct 10, 1997
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
240MG
Marketing Status: Discontinued
Active Ingredient: DILTIAZEM HYDROCHLORIDE
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 240MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074852
Product Number: 003
Approval Date: Oct 10, 1997
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: DILTIAZEM HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 240MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074852
Product Number: 003
Approval Date: Oct 10, 1997
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status: Discontinued
Patent and Exclusivity Information