MEGACE

Product NDC

0015-0508

11-digit product format

000150508

Labeler code

0015

Product ID

0015-0508_e1fc15a8-58f3-41f3-91ee-613a57b40499

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MEGESTROL ACETATE

Dosage form

SUSPENSION

Route

ORAL

Labeler

E.R. Squibb & Sons, L.L.C

Application

NDA020264

Marketing category

NDA

Marketing start

2009-06-01

Marketing end

2019-03-31

Substance

MEGESTROL ACETA

Active strength

40 mg/mL

Pharmacologic classes

Progesterone Co

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record