Fluphenazine Hydrochloride

Product NDC
53808-0600
11-digit product format
538080600
Labeler code
53808
Product ID
53808-0600_4589f1cd-5570-48bb-a94b-499faa06d4a1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FLUPHENAZINE HYDROCHLORIDE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
State of Florida DOH Central Pharmacy
Application
ANDA089804
Marketing category
ANDA
Marketing start
2009-07-01
Marketing end
0000-00-00
Substance
FLUPHENAZINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Phenothiazines [CS],Phenothiazine [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53808-0600-12021-01-15C16284748780-1956f9ecf-ca6b-621f-e053-dbdaa90a74ad69b5a8a7-03b1-41ad-b1ed-f922e3ab4bdd
53808-0600-12019-10-21C16284748780-1956f9ecf-ca6b-621f-e053-dbdaa90a74ad69b5a8a7-03b1-41ad-b1ed-f922e3ab4bdd