Dantrium - 42023-126-01 - (dantrolene sodium)

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Drug Information of Dantrium

Product NDC: 42023-126
Proprietary Name: Dantrium
Non Proprietary Name: dantrolene sodium
Active Ingredient(s): 100    mg/1 & nbsp;   dantrolene sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Dantrium

Product NDC: 42023-126
Labeler Name: JHP Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017443
Marketing Category: NDA
Start Marketing Date: 20080801

Package Information of Dantrium

Package NDC: 42023-126-01
Package Description: 100 CAPSULE in 1 BOTTLE (42023-126-01)

NDC Information of Dantrium

NDC Code 42023-126-01
Proprietary Name Dantrium
Package Description 100 CAPSULE in 1 BOTTLE (42023-126-01)
Product NDC 42023-126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dantrolene sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080801
Marketing Category Name NDA
Labeler Name JHP Pharmaceuticals LLC
Substance Name DANTROLENE SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Decreased Striated Muscle Contraction [PE],Decreased Striated Muscle Tone [PE],Skeletal Muscle Relaxant [EPC]

Complete Information of Dantrium


General Information