Carbidopa and Levodopa

Product NDC

63739-046

11-digit product format

637390046

Labeler code

63739

Product ID

63739-046_81781ad4-9303-4bf2-a3c5-7c338bf0cc3c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carbidopa and Levodopa

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA073618

Marketing category

ANDA

Marketing start

1993-03-01

Marketing end

0000-00-00

Substance

CARBIDOPA; LEVODOPA

Active strength

10 mg/1; mg/1

Pharmacologic classes

Aromatic Amino Acid [EPC],Amino Acids, Aromatic [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record