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"21130-191-20" National Drug Code (NDC)
Famotidine 200 TABLET in 1 BOTTLE (21130-191-20)
(SAFEWAY)
NDC Code
21130-191-20
Package Description
200 TABLET in 1 BOTTLE (21130-191-20)
Product NDC
21130-191
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230630
Marketing Category Name
ANDA
Application Number
ANDA215822
Manufacturer
SAFEWAY
Substance Name
FAMOTIDINE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21130-191-20