PROCHLORPERAZINE MALEATE

Product NDC
66267-318
11-digit product format
662670318
Labeler code
66267
Product ID
66267-318_b8a75396-f023-e6a1-e053-2995a90a0aa3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prochlorperazine maleate
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA040268
Marketing category
ANDA
Marketing start
1998-03-01
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
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-318-30EA - Each66267-31849236708-ec17-4364-940c-5d769a6846db12018-11-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66267-318-04662670318044 TABLET in 1 BOTTLE (66267-318-04) 4 tablet2018-10-300000-00-00NoNoCurrent
66267-318-106626703181010 TABLET in 1 BOTTLE (66267-318-10) 10 tablet2018-10-300000-00-00NoNoCurrent
66267-318-126626703181212 TABLET in 1 BOTTLE (66267-318-12) 12 tablet2018-10-300000-00-00NoNoCurrent
66267-318-156626703181515 TABLET in 1 BOTTLE (66267-318-15) 15 tablet2018-10-300000-00-00NoNoCurrent
66267-318-206626703182020 TABLET in 1 BOTTLE (66267-318-20) 20 tablet2018-10-300000-00-00NoNoCurrent
66267-318-306626703183030 TABLET in 1 BOTTLE (66267-318-30) 30 tablet2018-10-300000-00-00NoNoCurrent
66267-318-606626703186060 TABLET in 1 BOTTLE (66267-318-60) 60 tablet2018-10-300000-00-00NoNoCurrent