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"71205-535-10" National Drug Code (NDC)
Famotidine 10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)
(Proficient Rx LP)
NDC Code
71205-535-10
Package Description
10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)
Product NDC
71205-535
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20151222
Marketing Category Name
ANDA
Application Number
ANDA206530
Manufacturer
Proficient Rx LP
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/71205-535-10