Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020882

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NEURONTIN (GABAPENTIN)
600MG
Marketing Status: Prescription

Active Ingredient: GABAPENTIN
Proprietary Name: NEURONTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB1
Application Number: N020882
Product Number: 001
Approval Date: Oct 9, 1998
Applicant Holder Full Name: VIATRIS SPECIALTY LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

NEURONTIN (GABAPENTIN)
800MG
Marketing Status: Prescription

Active Ingredient: GABAPENTIN
Proprietary Name: NEURONTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 800MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB1
Application Number: N020882
Product Number: 002
Approval Date: Oct 9, 1998
Applicant Holder Full Name: VIATRIS SPECIALTY LLC
Marketing Status:  Prescription
Patent and Exclusivity Information