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"72865-214-30" National Drug Code (NDC)
Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)
(XLCare Pharmaceuticals, Inc.)
NDC Code
72865-214-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)
Product NDC
72865-214
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20211015
Marketing Category Name
ANDA
Application Number
ANDA215689
Manufacturer
XLCare 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/72865-214-30