basic care dual action complete

Product NDC
0113-7321
11-digit product format
001137321
Labeler code
0113
Product ID
0113-7321_e57f4fb8-894b-401f-9f65-e62a4f8e3315
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine, calcium carbonate and magnesium hydroxide
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
L. Perrigo Company
Application
ANDA077355
Marketing category
ANDA
Marketing start
2018-12-27
Marketing end
0000-00-00
Substance
FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE
Active strength
10 mg/1; mg/1; mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0113-7321-710011373217150 TABLET, CHEWABLE in 1 BOTTLE (0113-7321-71) 2018-12-270000-00-00NoNoCurrent