leader acid reducer complete

Product NDC
37205-680
11-digit product format
372050680
Labeler code
37205
Product ID
37205-680_3b473348-be73-405c-a7db-940d80727243
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine, calcium carbonate and magnesium hydroxide
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Cardinal Health
Application
ANDA077355
Marketing category
ANDA
Marketing start
2012-04-26
Marketing end
2019-05-31
Substance
FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-680-63EA - Each37205-6808d8ec742-46df-4e37-8e8b-6c410ae3d02a12014-07-02