"48433-015-20" National Drug Code (NDC)

NDC Code	48433-015-20
Package Description	100 BLISTER PACK in 1 CARTON (48433-015-20) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (48433-015-01)
Product NDC	48433-015
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbidopa And Levodopa
Non-Proprietary Name	Carbidopa And Levodopa
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20260313
Marketing Category Name	ANDA
Application Number	ANDA075091
Manufacturer	Safecor Health, LLC
Substance Name	CARBIDOPA HYDRATE; LEVODOPA
Strength	25; 100
Strength Unit	mg/1; mg/1
Pharmacy Classes	Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]