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CYCLOSERINE - 13845-1201-3 - (CYCLOSERINE)

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Drug Information of CYCLOSERINE

Product NDC: 13845-1201
Proprietary Name: CYCLOSERINE
Non Proprietary Name: CYCLOSERINE
Active Ingredient(s): 250    mg/250mg & nbsp;   CYCLOSERINE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of CYCLOSERINE

Product NDC: 13845-1201
Labeler Name: Purdue GMP Center LLC dba The Chao Center
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060593
Marketing Category: ANDA
Start Marketing Date: 20090301

Package Information of CYCLOSERINE

Package NDC: 13845-1201-3
Package Description: 40 CAPSULE in 1 BOTTLE (13845-1201-3) > 250 mg in 1 CAPSULE (13845-1201-1)

NDC Information of CYCLOSERINE

NDC Code 13845-1201-3
Proprietary Name CYCLOSERINE
Package Description 40 CAPSULE in 1 BOTTLE (13845-1201-3) > 250 mg in 1 CAPSULE (13845-1201-1)
Product NDC 13845-1201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CYCLOSERINE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090301
Marketing Category Name ANDA
Labeler Name Purdue GMP Center LLC dba The Chao Center
Substance Name CYCLOSERINE
Strength Number 250
Strength Unit mg/250mg
Pharmaceutical Classes

Complete Information of CYCLOSERINE


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