Leader Acid Reducer

Product NDC
37205-861
11-digit product format
372050861
Labeler code
37205
Product ID
37205-861_2b9e522e-88de-4f22-9a1a-e61e6928a2a6
Type
HUMAN OTC DRUG
Nonproprietary name
Famotidine
Dosage form
TABLET
Route
ORAL
Labeler
Cardinal Health
Application
ANDA077351
Marketing category
ANDA
Marketing start
2006-11-02
Marketing end
2021-01-30
Substance
FAMOTIDINE
Active strength
20 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record