Lidocaine Hydrochloride and Epinephrine

Product NDC
63739-468
11-digit product format
637390468
Labeler code
63739
Product ID
63739-468_3365c3d6-28a0-420d-89a7-9bc9b8539d4c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lidocaine hydrochloride anhydrous and epinephrine
Dosage form
INJECTION, SOLUTION
Route
INFILTRATION
Labeler
McKesson Packaging Services Business Unit of McKesson Corporation
Application
ANDA089644
Marketing category
ANDA
Marketing start
2010-05-03
Marketing end
0000-00-00
Substance
LIDOCAINE HYDROCHLORIDE ANHYDROUS; EPINEPHRINE
Active strength
10 mg/mL; ug/mL
Pharmacologic classes
Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE],Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
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
63739-468-052021-07-16C16284748780-1956f9ecf-d359-621f-e053-dbdaa90a74ad3365c3d6-28a0-420d-89a7-9bc9b8539d4c
63739-468-052019-10-21C16284748780-1956f9ecf-d359-621f-e053-dbdaa90a74ad3365c3d6-28a0-420d-89a7-9bc9b8539d4c