Carbidopa and Levodopa

Product NDC
71610-269
11-digit product format
716100269
Labeler code
71610
Product ID
71610-269_a51379dd-c47a-4fcd-aed0-5f19c18bf12c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbidopa and Levodopa
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA073589
Marketing category
ANDA
Marketing start
2018-07-16
Marketing end
0000-00-00
Substance
CARBIDOPA; LEVODOPA
Active strength
25 mg/1; mg/1
Pharmacologic classes
Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71610-269-60EA - Each71610-269053e28ac-4864-4aff-806d-f31bd7ff720212019-06-19
71610-269-80EA - Each71610-269cf393c17-0397-4d85-9bf2-37c7f54cb6b412019-06-19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71610-269CARBIDOPA AND LEVODOPA TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]1Legacy NDC20190515_eddc3e61-4fb3-4a2f-9102-406c5f397a64.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71610-269-607161002696090 TABLET in 1 BOTTLE (71610-269-60) 90 tablet2019-05-010000-00-00NoNoCurrent
71610-269-8071610026980180 TABLET in 1 BOTTLE (71610-269-80) 180 tablet2019-05-010000-00-00NoNoCurrent