Prochlorperazine Maleate

Product NDC
63629-1335
11-digit product format
636291335
Labeler code
63629
Product ID
63629-1335_031a89f5-305d-4f1b-942d-fce569d68fd0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prochlorperazine Maleate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
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
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
63629-1335-1EA - Each63629-13350ebd22ac-064d-4c4e-b2c4-cc94ed2b050812013-02-13
63629-1335-2EA - Each63629-1335195f927d-c6b7-444a-8a5e-b3e734c4b5ec12013-02-13
63629-1335-3EA - Each63629-13352b384972-2de1-41be-9d2f-3e5d10175ea512013-02-13
63629-1335-4EA - Each63629-1335f70bb400-54a0-46e2-b0fb-6dbb98c8382b12013-02-13
63629-1335-5EA - Each63629-13352091197c-62ec-4184-bed2-3e74f2f712b812013-02-13