Carbidopa and Levodopa

Product NDC

63739-048

11-digit product format

637390048

Labeler code

63739

Product ID

63739-048_51962452-1356-4b1e-99a8-3c22cace037c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Carbidopa and Levodopa

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA073607

Marketing category

ANDA

Marketing start

1993-01-01

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

2020-12-31

Current FDA listing

Historical FDA.report record