Prochlorperazine Maleate

Product NDC
0378-5110
11-digit product format
003785110
Labeler code
0378
Product ID
0378-5110_86370b37-2a3d-4231-92a8-640b467db17d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
prochlorperazine maleate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mylan Pharmaceuticals Inc.
Application
ANDA040185
Marketing category
ANDA
Marketing start
1996-11-18
Marketing end
2030-01-31
Substance
PROCHLORPERAZINE MALEATE
Active strength
10 mg/1
Pharmacologic classes
Phenothiazine [EPC],Phenothiazines [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9bfe4595-32b8-9175-3af8-875e9c4c0538Product name620260305
7335ddeb-6cbd-135c-487d-96fa4587ad65Product name620250331
a6ffe0a0-7823-b305-75e9-2a5c6f2be4acProduct name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0378-5110-01EA - Each0378-5110fa0f9276-215b-4ee5-87b6-c59ad9881b3612012-07-24

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198365prochlorperazine maleate 10 MG Oral TabletPSN3fb514f8-ea97-60ca-e054-00144ff8d46c12
198365prochlorperazine 10 MG Oral TabletSCD3fb514f8-ea97-60ca-e054-00144ff8d46c12
198365prochlorperazine (as prochlorperazine maleate) 10 MG Oral TabletSY3fb514f8-ea97-60ca-e054-00144ff8d46c12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0378-5110-0100378511001100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5110-01) 1996-11-180000-00-00NoNoCurrent