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"50436-7371-1" National Drug Code (NDC)
Famotidine 60 TABLET in 1 BOTTLE (50436-7371-1)
(Unit Dose Services)
NDC Code
50436-7371-1
Package Description
60 TABLET in 1 BOTTLE (50436-7371-1)
Product NDC
50436-7371
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20010416
Marketing Category Name
ANDA
Application Number
ANDA075805
Manufacturer
Unit Dose Services
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/50436-7371-1