Terazol 3

Product NDC
50458-531
11-digit product format
504580531
Labeler code
50458
Product ID
50458-531_9a055cd8-638b-11ea-a644-412efc2ca371
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
TERCONAZOLE
Dosage form
SUPPOSITORY
Route
VAGINAL
Labeler
Janssen Pharmaceuticals, Inc.
Application
NDA019641
Marketing category
NDA
Marketing start
1988-05-24
Marketing end
2020-06-15
Substance
TERCONAZOLE
Active strength
80 mg/1
Pharmacologic classes
Azole Antifungal [EPC],Azoles [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
50458-531-01EA - Each50458-53144994bc7-a73a-430e-948d-2055ff72540512014-09-03