Etodolac

Product NDC

55700-601

11-digit product format

557000601

Labeler code

55700

Product ID

55700-601_e8e6a958-79c5-4b91-ae26-3cda3b29ee93

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Etodolac

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA091134

Marketing category

ANDA

Marketing start

2018-04-13

Marketing end

0000-00-00

Substance

ETODOLAC

Active strength

500 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record