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"71335-2190-8" National Drug Code (NDC)
Famotidine 50 TABLET, FILM COATED in 1 BOTTLE (71335-2190-8)
(Bryant Ranch Prepack)
NDC Code
71335-2190-8
Package Description
50 TABLET, FILM COATED in 1 BOTTLE (71335-2190-8)
Product NDC
71335-2190
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220606
Marketing Category Name
ANDA
Application Number
ANDA216441
Manufacturer
Bryant Ranch Prepack
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/71335-2190-8