Carbidopa

Product NDC
63629-9193
11-digit product format
636299193
Labeler code
63629
Product ID
63629-9193_03a74a07-0806-4aa0-b5f3-3f989dfa67c1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbidopa
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA203261
Marketing category
ANDA
Marketing start
2014-03-10
Marketing end
0000-00-00
Substance
CARBIDOPA
Active strength
25 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-9193-1EA - Each63629-9193553b896f-176a-4960-a5ed-78b23318d93b12022-09-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-9193-163629919301100 TABLET in 1 BOTTLE (63629-9193-1) 100 tablet2022-08-030000-00-00NoNoCurrent