Lidocaine Hydrochloride and Epinephrine Bitartrate

Product NDC
51004-2010
11-digit product format
510042010
Labeler code
51004
Product ID
51004-2010_ba7ff05c-cdd8-4f17-a908-8e847ea35a75
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine Hydrochloride and Epinephrine Bitartrate
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Labeler
Novocol Pharmaceutical of Canada, Inc.
Application
ANDA088390
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
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51004-2010-52024-12-27C16284748780-197449f38-c13a-f6ea-e053-dbdaa90aa703e38e35cc-f8d2-41ad-9477-748461aef348
51004-2010-52019-11-13C16284748780-197449f38-c13a-f6ea-e053-dbdaa90aa703e38e35cc-f8d2-41ad-9477-748461aef348