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"51655-312-25" National Drug Code (NDC)
Famotidine 60 TABLET in 1 BOTTLE, PLASTIC (51655-312-25)
(Northwind Pharmaceuticals, LLC)
NDC Code
51655-312-25
Package Description
60 TABLET in 1 BOTTLE, PLASTIC (51655-312-25)
Product NDC
51655-312
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200521
Marketing Category Name
ANDA
Application Number
ANDA075805
Manufacturer
Northwind Pharmaceuticals, 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/51655-312-25