Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 017443

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DANTRIUM (DANTROLENE SODIUM)
25MG
Marketing Status: Prescription

Active Ingredient: DANTROLENE SODIUM
Proprietary Name: DANTRIUM
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 25MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N017443
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PAR STERILE PRODUCTS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

DANTRIUM (DANTROLENE SODIUM)
50MG
Marketing Status: Prescription

Active Ingredient: DANTROLENE SODIUM
Proprietary Name: DANTRIUM
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 50MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N017443
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PAR STERILE PRODUCTS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

DANTRIUM (DANTROLENE SODIUM)
100MG
Marketing Status: Prescription

Active Ingredient: DANTROLENE SODIUM
Proprietary Name: DANTRIUM
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 100MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N017443
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PAR STERILE PRODUCTS LLC
Marketing Status:  Prescription
Patent and Exclusivity Information