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"68001-398-03" National Drug Code (NDC)
Famotidine 500 TABLET, FILM COATED in 1 BOTTLE (68001-398-03)
(BluePoint Laboratories)
NDC Code
68001-398-03
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (68001-398-03)
Product NDC
68001-398
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190619
Marketing Category Name
ANDA
Application Number
ANDA206530
Manufacturer
BluePoint Laboratories
Substance Name
FAMOTIDINE
Strength
40
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/68001-398-03