Chlorpromazine Hydrochloride

Product NDC
51079-130
11-digit product format
510790130
Labeler code
51079
Product ID
51079-130_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
ANDA084113
Marketing category
ANDA
Marketing start
1994-11-23
Marketing end
2020-08-31
Substance
CHLORPROMAZINE HYDROCHLORIDE
Active strength
50 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
51079-130-01EA - Each51079-130bca6cd64-2e86-444e-8329-58b588dca39b12012-07-24
51079-130-20EA - Each51079-130ce6679cd-f4eb-4227-b3a0-e543f20f298112012-07-24