Trifluoperazine Hydrochloride

Product NDC
0781-1034
11-digit product format
007811034
Labeler code
0781
Product ID
0781-1034_5a97a496-6669-4b98-a2e8-e87b8c7d556a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trifluoperazine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA085789
Marketing category
ANDA
Marketing start
1981-11-20
Marketing end
0000-00-00
Substance
TRIFLUOPERAZINE HYDROCHLORIDE
Active strength
5 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
0781-1034-01EA - Each0781-103441667a07-2ef6-4352-b94c-a551ab08a95f12012-07-24