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Dantrolene Sodium - 0115-4411-01 - (Dantrolene Sodium)

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Drug Information of Dantrolene Sodium

Product NDC: 0115-4411
Proprietary Name: Dantrolene Sodium
Non Proprietary Name: Dantrolene Sodium
Active Ingredient(s): 25    mg/1 & nbsp;   Dantrolene Sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Dantrolene Sodium

Product NDC: 0115-4411
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076856
Marketing Category: ANDA
Start Marketing Date: 20050301

Package Information of Dantrolene Sodium

Package NDC: 0115-4411-01
Package Description: 100 CAPSULE in 1 BOTTLE (0115-4411-01)

NDC Information of Dantrolene Sodium

NDC Code 0115-4411-01
Proprietary Name Dantrolene Sodium
Package Description 100 CAPSULE in 1 BOTTLE (0115-4411-01)
Product NDC 0115-4411
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dantrolene Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050301
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name DANTROLENE SODIUM
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC]

Complete Information of Dantrolene Sodium


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