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Thiothixene - 51079-589-20 - (thiothixene)

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Drug Information of Thiothixene

Product NDC: 51079-589
Proprietary Name: Thiothixene
Non Proprietary Name: thiothixene
Active Ingredient(s): 10    mg/1 & nbsp;   thiothixene
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Thiothixene

Product NDC: 51079-589
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071093
Marketing Category: ANDA
Start Marketing Date: 20121205

Package Information of Thiothixene

Package NDC: 51079-589-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-589-20) > 1 CAPSULE in 1 BLISTER PACK (51079-589-01)

NDC Information of Thiothixene

NDC Code 51079-589-20
Proprietary Name Thiothixene
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-589-20) > 1 CAPSULE in 1 BLISTER PACK (51079-589-01)
Product NDC 51079-589
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name thiothixene
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121205
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name THIOTHIXENE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Typical Antipsychotic [EPC]

Complete Information of Thiothixene


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