Quetiapine Fumarate

Product NDC
34908-637
11-digit product format
349080637
Labeler code
34908
Product ID
34908-637_781f6242-bc94-424b-be23-ea9eb61c0889
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
quetiapine fumarate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Novast Laboratories, Ltd.
Application
ANDA208947
Marketing category
ANDA
Marketing start
2017-08-31
Substance
QUETIAPINE FUMARATE
Active strength
200 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Quetiapine Fumarate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
QUETIAPINE FUMARATE200 mg/1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
34908-637-10349080637101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (34908-637-10) 2017-08-310000-00-00NoNoCurrent
34908-637-303490806373030 TABLET, EXTENDED RELEASE in 1 BOTTLE (34908-637-30) 2017-08-310000-00-00NoNoCurrent
34908-637-603490806376060 TABLET, EXTENDED RELEASE in 1 BOTTLE (34908-637-60) 2017-08-310000-00-00NoNoCurrent
34908-637-903490806379090 TABLET, EXTENDED RELEASE in 1 BOTTLE (34908-637-90) 2017-08-310000-00-00NoNoCurrent