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Quetiapine fumarate - 49349-975-24 - (Quetiapine fumarate)

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Drug Information of Quetiapine fumarate

Product NDC: 49349-975
Proprietary Name: Quetiapine fumarate
Non Proprietary Name: Quetiapine fumarate
Active Ingredient(s): 200    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: 49349-975
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202152
Marketing Category: ANDA
Start Marketing Date: 20130215

Package Information of Quetiapine fumarate

Package NDC: 49349-975-24
Package Description: 200 TABLET, FILM COATED in 1 CANISTER (49349-975-24)

NDC Information of Quetiapine fumarate

NDC Code 49349-975-24
Proprietary Name Quetiapine fumarate
Package Description 200 TABLET, FILM COATED in 1 CANISTER (49349-975-24)
Product NDC 49349-975
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine fumarate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130215
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name QUETIAPINE FUMARATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Quetiapine fumarate


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