Lidocaine

Product NDC
31382-262
11-digit product format
313820262
Labeler code
31382
Product ID
31382-262_31b772b2-a127-43d4-9f60-fe6e7460ae63
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine Hydrochloride and Epinephrine Bitartrate
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Labeler
CareStream Health, Inc.
Application
ANDA088389
Marketing category
ANDA
Marketing start
2011-11-07
Marketing end
0000-00-00
Substance
LIDOCAINE HYDROCHLORIDE; EPINEPHRINE BITARTRATE
Active strength
20 mg/mL; mg/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
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
31382-262-052024-12-20C16284748780-19d75b9d0-1864-f424-e053-dadaa90a57ce4fff6849-8a45-41f2-a411-9cf8aa685969
31382-262-052020-01-31C16284748780-19d75b9d0-1864-f424-e053-dadaa90a57ce4fff6849-8a45-41f2-a411-9cf8aa685969