Prochlorperazine Maleate

Product NDC
51079-542
11-digit product format
510790542
Labeler code
51079
Product ID
51079-542_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
2020-04-30
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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-542-01EA - Each51079-542aaa1c631-45f2-4e47-bd9f-926b97035e8112012-07-24
51079-542-20EA - Each51079-542c567058c-8873-4ca8-b606-9ae660505f7212012-07-24