Lidocaine Hydrochloride

Product NDC
17856-6002
11-digit product format
178566002
Labeler code
17856
Product ID
17856-6002_a87d9775-c7ae-4c19-957c-b9f1b318f34d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine Hydrochloride
Dosage form
SOLUTION
Route
OROPHARYNGEAL
Labeler
ATLANTIC BIOLOGICALS CORP.
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
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
17856-6002-11785660020172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-6002-1) > 10 mL in 1 CUP, UNIT-DOSE (17856-6002-5) 2022-09-210000-00-00NoNoCurrent
17856-6002-21785660020250 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-6002-2) > 15 mL in 1 CUP, UNIT-DOSE (17856-6002-6) 2022-09-210000-00-00NoNoCurrent
17856-6002-31785660020350 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-6002-3) > 20 mL in 1 CUP, UNIT-DOSE (17856-6002-7) 2022-09-210000-00-00NoNoCurrent
17856-6002-41785660020472 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-6002-4) > 5 mL in 1 CUP, UNIT-DOSE (17856-6002-8) 2022-09-210000-00-00NoNoCurrent