FDA.reportPublic FDA data

Carbidopa and levodopa

Product NDC
42291-471
11-digit product format
422910471
Labeler code
42291
Product ID
42291-471_485d7c0e-be0a-f880-e063-6294a90aacb8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbidopa and levodopa
Dosage form
TABLET
Route
ORAL
Labeler
AvKARE
Application
ANDA074260
Marketing category
ANDA
Marketing start
2022-06-24
Substance
CARBIDOPA; LEVODOPA
Active strength
10; 100 mg/1; mg/1
Pharmacologic classes
Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Carbidopa and levodopa
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CARBIDOPA10 mg/1
LEVODOPA100 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiMNX7R8C5VO, 46627O600J
Rxcui197443

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5ce6fab2-d006-4589-8ba0-02cee499cc60Product name220260128
ebf3b793-6fcd-797b-9d2e-c3faf6d29442Product name520251106
162160fe-5ea6-4f9d-aa38-c4b780c57046Product name120250515
0e5ae331-9620-4d1f-8061-7c437c7f1c42Product name120250312
028fdaca-77da-0dfe-e445-7dfc440fc97eProduct name420250224
7d015b89-35e8-b484-e5db-c0c44814f63cProduct name720241218
de702a02-e9c0-4daf-9101-e44f2c0d4e66Product name120220609
681917df-580c-4199-896d-b739fbb25ed3Product name120190412
7d015b89-35e8-b484-e5db-c0c44814f63cProduct name420171212
1fa100ae-9ab3-4df0-afe7-33ab01fd4a41Product name120150313
88839c8d-b65b-4a50-997b-4c74539855ffProduct name120150313

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42291-471-012024-11-04C16284748780-11030e365-6f51-111a-e063-dadaa90a10e2Carbidopa and Levodopa Tablets, USP
42291-471-502024-11-04C16284748780-11030e365-6f51-111a-e063-dadaa90a10e2Carbidopa and Levodopa Tablets, USP
42291-471-012024-01-30C16284748780-11030e365-6f51-111a-e063-dadaa90a10e2Carbidopa and Levodopa Tablets, USP
42291-471-502024-01-30C16284748780-11030e365-6f51-111a-e063-dadaa90a10e2Carbidopa and Levodopa Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42291-471-01Carbidopa and levodopa100 in 1 BOTTLETABLET1003
42291-471-50Carbidopa and levodopa500 in 1 BOTTLETABLET5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42291-471CARBIDOPA AND LEVODOPA TABLET [AVKARE]2Current NDC, Legacy NDC, 2 package rows20241105_e232e055-7892-3541-e053-2995a90a1e74.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197443carbidopa 10 MG / levodopa 100 MG Oral TabletPSNe232e055-7892-3541-e053-2995a90a1e743
197443carbidopa 10 MG / levodopa 100 MG Oral TabletSCDe232e055-7892-3541-e053-2995a90a1e743
197443carbidopa (as carbidopa monohydrate) 10 MG / levodopa 100 MG Oral TabletSYe232e055-7892-3541-e053-2995a90a1e743
197443Carbidopa 10 MG / L-DOPA 100 MG Oral TabletSYe232e055-7892-3541-e053-2995a90a1e743

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42291-471-0142291047101100 TABLET in 1 BOTTLE (42291-471-01) 100 tablet2022-06-240000-00-00NoNoCurrent
42291-471-5042291047150500 TABLET in 1 BOTTLE (42291-471-50) 500 tablet2022-06-240000-00-00NoNoCurrent