Chlorpromazine Hydrochloride

Product NDC
51079-516
11-digit product format
510790516
Labeler code
51079
Product ID
51079-516_9a252b62-8427-382e-e053-2995a90a3222
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Chlorpromazine Hydrochloride
Dosage form
TABLET, SUGAR COATED
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA084114
Marketing category
ANDA
Marketing start
1994-11-28
Marketing end
2020-08-31
Substance
CHLORPROMAZINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Phenothiazines [CS],Phenothiazine [EPC]
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
51079-516-01EA - Each51079-5160c66122f-9205-443a-942f-aa683420153712012-07-24
51079-516-20EA - Each51079-516d829b26a-2f19-48d9-9165-39efc38b3e2912012-07-24