Prochlorperazine Maleate

Product NDC
42708-048
11-digit product format
427080048
Labeler code
42708
Product ID
42708-048_7ca4d17a-d9b7-4ea9-8fc6-6e4086fa0890
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prochlorperazine Maleate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
QPharma Inc
Application
ANDA040120
Marketing category
ANDA
Marketing start
1996-07-25
Marketing end
0000-00-00
Substance
PROCHLORPERAZINE MALEATE
Active strength
10 mg/1
Pharmacologic classes
Phenothiazine [EPC],Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42708-048-602021-03-12C16284748780-1ba0f9c33-2629-a910-e053-dadaa90a0b859a9bddf2-6df6-406d-aeed-e234565fdd83
42708-048-602021-01-29C16284748780-1ba0f9c33-2629-a910-e053-dadaa90a0b859a9bddf2-6df6-406d-aeed-e234565fdd83