Acid Controller Complete

Product NDC
0363-0321
11-digit product format
003630321
Labeler code
0363
Product ID
0363-0321_099ecf94-2673-4bca-bac1-48c3b39be01b
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine, calcium carbonate and magnesium hydroxide
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Walgreen Company
Application
ANDA077355
Marketing category
ANDA
Marketing start
2008-07-30
Marketing end
0000-00-00
Substance
FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Active strength
10 mg/1; mg/1; mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0321-63EA - Each0363-0321e7b76155-7580-4dea-8ca7-32256c2d125212012-07-24
0363-0321-71EA - Each0363-032149679461-fffd-4ab5-b754-21e04a0a6f0f12014-10-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0363-0321-630036303216325 TABLET, CHEWABLE in 1 BOTTLE (0363-0321-63) 2008-07-310000-00-00NoNoCurrent
0363-0321-650036303216530 TABLET, CHEWABLE in 1 BOTTLE (0363-0321-65) 2008-11-120000-00-00NoNoCurrent
0363-0321-710036303217150 TABLET, CHEWABLE in 1 BOTTLE (0363-0321-71) 2013-08-190000-00-00NoNoCurrent