Trifluoperazine Hydrochloride

Product NDC
35356-823
11-digit product format
353560823
Labeler code
35356
Product ID
35356-823_55a9cb2a-2c00-4e4a-adce-d48cc6ce1b23
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
trifluoperazine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA040209
Marketing category
ANDA
Marketing start
2012-08-22
Marketing end
0000-00-00
Substance
TRIFLUOPERAZINE HYDROCHLORIDE
Active strength
1 mg/1
Pharmacologic classes
Phenothiazine [EPC],Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-823-30EA - Each35356-8233d1a62a5-ca58-48cc-bd88-6636224b3e8e12013-07-02