Carbidopa and Levodopa

Product NDC

51079-884

11-digit product format

510790884

Labeler code

51079

Product ID

51079-884_95fa0a59-5e1c-aa1a-e053-2a95a90a5334

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

carbidopa and levodopa

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA090324

Marketing category

ANDA

Marketing start

2010-01-27

Marketing end

2020-08-31

Substance

CARBIDOPA; LEVODOPA

Active strength

25 mg/1; mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record