Lidocaine Hydrochloride

Product NDC
63739-694
11-digit product format
637390694
Labeler code
63739
Product ID
63739-694_acf79600-f78d-469e-a8a4-0ae3616ed2d9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine Hydrochloride
Dosage form
SOLUTION
Route
OROPHARYNGEAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA040708
Marketing category
ANDA
Marketing start
2007-02-27
Marketing end
0000-00-00
Substance
LIDOCAINE HYDROCHLORIDE ANHYDROUS
Active strength
20 mg/mL
Pharmacologic classes
Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-694-572020-07-22C16284748780-1ab0e2407-2b36-f274-e053-dbdaa90a647153c6be5d-9fdc-4558-968e-3eb9721bfae4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-694-57ML - Milliliter63739-694d4444182-294c-4330-ad25-21cf88db5c1512014-10-03