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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 010596

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CELONTIN (METHSUXIMIDE)
300MG
Marketing Status: Prescription
Active Ingredient: METHSUXIMIDE
Proprietary Name: CELONTIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N010596
Product Number: 008
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Prescription
Patent and Exclusivity Information
CELONTIN (METHSUXIMIDE)
150MG
Marketing Status: Discontinued
Active Ingredient: METHSUXIMIDE
Proprietary Name: CELONTIN
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N010596
Product Number: 007
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:  Discontinued
Patent and Exclusivity Information
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