Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020506

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TIAMATE (DILTIAZEM MALATE)
EQ 120MG HYDROCHLORIDE
Marketing Status: Discontinued

Active Ingredient: DILTIAZEM MALATE
Proprietary Name: TIAMATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 120MG HYDROCHLORIDE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020506
Product Number: 001
Approval Date: Oct 4, 1996
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

TIAMATE (DILTIAZEM MALATE)
EQ 180MG HYDROCHLORIDE
Marketing Status: Discontinued

Active Ingredient: DILTIAZEM MALATE
Proprietary Name: TIAMATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 180MG HYDROCHLORIDE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020506
Product Number: 002
Approval Date: Oct 4, 1996
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

TIAMATE (DILTIAZEM MALATE)
EQ 240MG HYDROCHLORIDE
Marketing Status: Discontinued

Active Ingredient: DILTIAZEM MALATE
Proprietary Name: TIAMATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 240MG HYDROCHLORIDE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N020506
Product Number: 003
Approval Date: Oct 4, 1996
Applicant Holder Full Name: MERCK AND CO INC
Marketing Status:  Discontinued
Patent and Exclusivity Information