leader acid reducer complete

Product NDC

37205-681

11-digit product format

372050681

Labeler code

37205

Product ID

37205-681_e825d6aa-f9b8-4aed-8757-125105853f81

Type

HUMAN OTC DRUG

Nonproprietary name

Famotidine, Calcium Carbonate, Magnesium Hydroxide

Dosage form

TABLET, CHEWABLE

Route

ORAL

Labeler

Cardinal Health

Application

ANDA077355

Marketing category

ANDA

Marketing start

2012-05-02

Marketing end

2020-02-29

Substance

FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE

Active strength

10 mg/1; mg/1; mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record