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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021698

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ZANTAC 150 (RANITIDINE HYDROCHLORIDE)
EQ 150MG BASE
Marketing Status: Discontinued
Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: ZANTAC 150
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N021698
Product Number: 001
Approval Date: Aug 31, 2004
Applicant Holder Full Name: CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE
Marketing Status:  Discontinued
Patent and Exclusivity Information
ZANTAC 150 (RANITIDINE HYDROCHLORIDE)
EQ 150MG BASE
Marketing Status: Discontinued
Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: ZANTAC 150
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N021698
Product Number: 002
Approval Date: Mar 13, 2007
Applicant Holder Full Name: CHATTEM INC DBA SANOFI CONSUMER HEALTHCARE
Marketing Status:  Discontinued
Patent and Exclusivity Information
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