Fluphenazine hydrochloride

Product NDC
51079-485
11-digit product format
510790485
Labeler code
51079
Product ID
51079-485_9c31c47b-4f7b-4800-e053-2a95a90ac060
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluphenazine hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA089804
Marketing category
ANDA
Marketing start
1998-04-30
Marketing end
2020-06-30
Substance
FLUPHENAZINE HYDROCHLORIDE
Active strength
1 mg/1
Pharmacologic classes
Phenothiazines [CS],Phenothiazine [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-485-01EA - Each51079-485f25b8a07-9dde-4a5f-a89b-cc44500c270f12012-07-24
51079-485-20EA - Each51079-48528d2099f-0182-41ff-aebc-2e60c3ab206112012-07-24