Terbinafine Hydrochloride

Product NDC
0536-1117
11-digit product format
005361117
Labeler code
0536
Product ID
0536-1117_0d3f2f7b-3be8-4d67-95f8-5adddc0f06e8
Type
HUMAN OTC DRUG
Nonproprietary name
Terbinafine Hydrochloride
Dosage form
CREAM
Route
TOPICAL
Labeler
Rugby Laboratories, Inc.
Application
ANDA077511
Marketing category
ANDA
Marketing start
2007-07-02
Marketing end
2020-09-30
Substance
TERBINAFINE HYDROCHLORIDE
Active strength
1 g/100g
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
0536-1117-28GM - Gram0536-11174c3ee977-1335-4ada-9c9c-5a6a9d386f6912017-06-15