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"58602-859-34" National Drug Code (NDC)
Famotidine 1 BOTTLE in 1 CARTON (58602-859-34) > 200 TABLET, FILM COATED in 1 BOTTLE
(Aurohealth LLC)
NDC Code
58602-859-34
Package Description
1 BOTTLE in 1 CARTON (58602-859-34) > 200 TABLET, FILM COATED in 1 BOTTLE
Product NDC
58602-859
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210302
Marketing Category Name
ANDA
Application Number
ANDA206531
Manufacturer
Aurohealth LLC
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/58602-859-34