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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 006002

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ARALEN HYDROCHLORIDE (CHLOROQUINE HYDROCHLORIDE)
EQ 40MG BASE/ML
Marketing Status: Discontinued
Active Ingredient: CHLOROQUINE HYDROCHLORIDE
Proprietary Name: ARALEN HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 40MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N006002
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
ARALEN (CHLOROQUINE PHOSPHATE)
500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: CHLOROQUINE PHOSPHATE
Proprietary Name: ARALEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N006002
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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