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Active Ingredient: GABAPENTIN
Proprietary Name: GABAPENTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB1
Application Number: A075694
Product Number: 001
Approval Date: Oct 21, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: GABAPENTIN
Proprietary Name: GABAPENTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 800MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB1
Application Number: A075694
Product Number: 002
Approval Date: Oct 21, 2004
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
