Prochlorperazine Maleate

Product NDC
51079-541
11-digit product format
510790541
Labeler code
51079
Product ID
51079-541_9b049a10-75a7-e1ef-e053-2a95a90aaf77
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
prochlorperazine maleate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA040185
Marketing category
ANDA
Marketing start
1997-04-15
Marketing end
2020-01-31
Substance
PROCHLORPERAZINE MALEATE
Active strength
5 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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-541-01EA - Each51079-54122c58308-b145-41e4-b71e-bd2fd24804a912012-07-24
51079-541-20EA - Each51079-541722587be-dd44-41bc-b722-ca1e4ccf033812012-07-24