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"53002-2199-5" National Drug Code (NDC)
Famotidine 15 TABLET, FILM COATED in 1 BOTTLE (53002-2199-5)
(RPK Pharmaceuticals, Inc.)
NDC Code
53002-2199-5
Package Description
15 TABLET, FILM COATED in 1 BOTTLE (53002-2199-5)
Product NDC
53002-2199
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
RPK Pharmaceuticals, Inc.
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/53002-2199-5