Fluphenazine Hydrochloride

Product NDC
70518-0318
11-digit product format
705180318
Labeler code
70518
Product ID
70518-0318_e11e019a-e8e4-379d-e053-2a95a90abd20
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Fluphenazine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA089743
Marketing category
ANDA
Marketing start
2017-03-15
Marketing end
0000-00-00
Substance
FLUPHENAZINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Phenothiazine [EPC], Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-0318-07051803180030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0318-0) 2017-03-150000-00-00NoNoCurrent
70518-0318-170518031801100 POUCH in 1 BOX (70518-0318-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-0318-2) 100 pouch2019-10-020000-00-00NoNoCurrent
70518-0318-37051803180330 TABLET, FILM COATED in 1 BLISTER PACK (70518-0318-3) 2020-06-080000-00-00NoNoCurrent
70518-0318-470518031804100 POUCH in 1 BOX (70518-0318-4) > 1 TABLET, FILM COATED in 1 POUCH (70518-0318-5) 100 pouch2021-01-070000-00-00NoNoCurrent