Lidocaine

Product NDC
17856-3008
11-digit product format
178563008
Labeler code
17856
Product ID
17856-3008_3633c32a-f772-258d-e063-6394a90a5c44
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lidocaine
Dosage form
OINTMENT
Route
TOPICAL
Labeler
ATLANTIC BIOLOGICALS CORP.
Application
ANDA086724
Marketing category
ANDA
Marketing start
1981-08-17
Substance
LIDOCAINE
Active strength
50 mg/g
Pharmacologic classes
Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lidocaine
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LIDOCAINE50 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii98PI200987
Rxcui1543069

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17856-3008-12025-03-28C16284748780-1f386c64a-1df3-0266-e053-dadaa90a7c1aLIDOCAINE OINTMENT USP, 5% (Spearmint Flavored)
17856-3008-12023-01-30C16284748780-1f386c64a-1df3-0266-e053-dadaa90a7c1aLIDOCAINE OINTMENT USP, 5% (Spearmint Flavored)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-3008-1Lidocaine120 in 1 BOX, UNIT-DOSEOINTMENT1204
17856-3008-1Lidocaine1 g in 1 SYRINGEOINTMENT14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-3008LIDOCAINE OINTMENT [ATLANTIC BIOLOGICALS CORP.]3Current NDC, Legacy NDC, 2 package rows20250331_1e8239f6-8d53-4b04-8bf8-c2cefe3ab5c3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1543069lidocaine 5 % Topical OintmentPSN1e8239f6-8d53-4b04-8bf8-c2cefe3ab5c34
1543069lidocaine 0.05 MG/MG Topical OintmentSCD1e8239f6-8d53-4b04-8bf8-c2cefe3ab5c34
1543069lidocaine 5 % Topical OintmentSY1e8239f6-8d53-4b04-8bf8-c2cefe3ab5c34

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17856-3008-117856300801120 SYRINGE in 1 BOX, UNIT-DOSE (17856-3008-1) / 1 g in 1 SYRINGE120 syringe2021-01-260000-00-00NoNoCurrent