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Active Ingredient: ZALCITABINE
Proprietary Name: HIVID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.375MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: N020199
Product Number: 001
Approval Date: Jun 19, 1992
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: ZALCITABINE
Proprietary Name: HIVID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.75MG
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: N020199
Product Number: 002
Approval Date: Jun 19, 1992
Applicant Holder Full Name: HOFFMANN LA ROCHE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
