leader acid reducer

Product NDC
37205-614
11-digit product format
372050614
Labeler code
37205
Product ID
37205-614_88b9838a-ab5e-4dd0-9ef9-b65d251269b4
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET
Route
ORAL
Labeler
Cardinal Health
Application
ANDA075400
Marketing category
ANDA
Marketing start
2009-10-14
Marketing end
2022-02-28
Substance
FAMOTIDINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37205-614-65372050614653 BLISTER PACK in 1 CARTON (37205-614-65) > 10 TABLET in 1 BLISTER PACK3 blister pack2009-10-140000-00-00NoNoCurrent