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Quetiapine Fumarate - 67877-246-38 - (Quetiapine Fumarate)

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Drug Information of Quetiapine Fumarate

Product NDC: 67877-246
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
Coding System: National Drug Codes(NDC)

Labeler Information of Quetiapine Fumarate

Product NDC: 67877-246
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201504
Marketing Category: ANDA
Start Marketing Date: 20130301

Package Information of Quetiapine Fumarate

Package NDC: 67877-246-38
Package Description: 10 BLISTER PACK in 1 CARTON (67877-246-38) > 10 TABLET in 1 BLISTER PACK (67877-246-33)

NDC Information of Quetiapine Fumarate

NDC Code 67877-246-38
Proprietary Name Quetiapine Fumarate
Package Description 10 BLISTER PACK in 1 CARTON (67877-246-38) > 10 TABLET in 1 BLISTER PACK (67877-246-33)
Product NDC 67877-246
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Quetiapine Fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130301
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
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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