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Quetiapine Fumarate - 52125-631-02 - (Quetiapine Fumarate)

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Drug Information of Quetiapine Fumarate

Product NDC: 52125-631
Proprietary Name: Quetiapine Fumarate
Non Proprietary Name: Quetiapine Fumarate
Active Ingredient(s): 100    mg/1 & nbsp;   Quetiapine Fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Quetiapine Fumarate

Product NDC: 52125-631
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077745
Marketing Category: ANDA
Start Marketing Date: 20130529

Package Information of Quetiapine Fumarate

Package NDC: 52125-631-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-631-02)

NDC Information of Quetiapine Fumarate

NDC Code 52125-631-02
Proprietary Name Quetiapine Fumarate
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-631-02)
Product NDC 52125-631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine Fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130529
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name QUETIAPINE FUMARATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine Fumarate


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