Lidocaine

Product NDC
70518-0854
11-digit product format
705180854
Labeler code
70518
Product ID
70518-0854_67f3099f-ac05-3b2b-e053-2a91aa0abe00
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine
Dosage form
OINTMENT
Route
TOPICAL
Labeler
REMEDYREPACK INC.
Application
ANDA040911
Marketing category
ANDA
Marketing start
2018-03-21
Marketing end
0000-00-00
Substance
LIDOCAINE
Active strength
5 g/100g
Pharmacologic classes
Amide Local Anesthetic [EPC],Amides [CS],Antiarrhythmic [EPC],Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-0854-02021-04-21C16284748780-19d75b9d0-11f8-f424-e053-dadaa90a57ce7ec46396-c36f-41ff-a940-755419fadeb3
70518-0854-02020-01-31C16284748780-19d75b9d0-11f8-f424-e053-dadaa90a57ce7ec46396-c36f-41ff-a940-755419fadeb3