Lidocaine Hydrochloride

Product NDC
58980-822
11-digit product format
589800822
Labeler code
58980
Product ID
58980-822_adb7a8f8-57b9-426c-a1e5-6d0285d85f10
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine Hydrochloride
Dosage form
LOTION
Route
TOPICAL
Labeler
Stratus Pharamceuticals
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-03-01
Marketing end
0000-00-00
Substance
LIDOCAINE HYDROCHLORIDE
Active strength
5 mL/177mL
Pharmacologic classes
Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58980-822-602021-03-03C16284748780-197449f38-c446-f6ea-e053-dbdaa90aa7031d043145-e897-4f5f-8724-b331a43c994e
58980-822-602019-11-13C16284748780-197449f38-c446-f6ea-e053-dbdaa90aa7031d043145-e897-4f5f-8724-b331a43c994e

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58980-822-60ML - Milliliter58980-822e87e9707-5227-487c-a635-d716fe69c47412012-07-24