Terbinafine Hydrochloride

Product NDC
37205-941
11-digit product format
372050941
Labeler code
37205
Product ID
37205-941_99993239-566c-4203-afc1-22c7438d4155
Type
HUMAN OTC DRUG
Nonproprietary name
Terbinafine Hydrochloride
Dosage form
CREAM
Route
TOPICAL
Labeler
Cardinal Health
Application
ANDA077511
Marketing category
ANDA
Marketing start
2007-07-02
Marketing end
2020-05-31
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
37205-941-992020-02-03C16284748780-19d75b9d0-dc15-f424-e053-dadaa90a57ced99dc2ad-ecc9-4a0a-a45e-a9655d71bf34
37205-941-992020-01-31C16284748780-19d75b9d0-dc15-f424-e053-dadaa90a57ced99dc2ad-ecc9-4a0a-a45e-a9655d71bf34

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-941-99GM - Gram37205-941c1ee3165-39d0-49d5-bafc-ddc07539c03012012-07-24