"51079-923-20" National Drug Code (NDC)

NDC Code	51079-923-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-923-20) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (51079-923-01)
Product NDC	51079-923
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	19991201
Marketing Category Name	ANDA
Application Number	ANDA075091
Manufacturer	Mylan Institutional Inc.
Substance Name	CARBIDOPA; LEVODOPA
Strength	50; 200
Strength Unit	mg/1; mg/1
Pharmacy Classes	Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]