CARBIDOPA AND LEVODOPA

Product NDC

51862-077

11-digit product format

518620077

Labeler code

51862

Product ID

51862-077_34c0f632-3f88-47cc-971a-f710ad62f939

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

CARBIDOPA and LEVODOPA

Dosage form

TABLET

Route

ORAL

Labeler

Mayne Pharma Inc

Application

ANDA073618

Marketing category

ANDA

Marketing start

2016-10-24

Marketing end

2020-03-31

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

0000-00-00

Current FDA listing

Historical FDA.report record