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"60687-595-01" National Drug Code (NDC)
Famotidine 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-595-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-595-11)
(American Health Packaging)
NDC Code
60687-595-01
Package Description
100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-595-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-595-11)
Product NDC
60687-595
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20210309
Marketing Category Name
ANDA
Application Number
ANDA206530
Manufacturer
American Health Packaging
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/60687-595-01