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"61919-281-20" National Drug Code (NDC)
Famotidine 20 TABLET in 1 BOTTLE (61919-281-20)
(Direct_Rx)
NDC Code
61919-281-20
Package Description
20 TABLET in 1 BOTTLE (61919-281-20)
Product NDC
61919-281
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190808
Marketing Category Name
ANDA
Application Number
ANDA075805
Manufacturer
Direct_Rx
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/61919-281-20