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"68001-240-00" National Drug Code (NDC)
Famotidine 100 TABLET in 1 BOTTLE (68001-240-00)
(BluePoint Laboratories)
NDC Code
68001-240-00
Package Description
100 TABLET in 1 BOTTLE (68001-240-00)
Product NDC
68001-240
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160129
End Marketing Date
20220531
Marketing Category Name
ANDA
Application Number
ANDA078916
Manufacturer
BluePoint Laboratories
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/68001-240-00