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"67877-842-01" National Drug Code (NDC)
Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01)
(Ascend Laboratories, LLC)
NDC Code
67877-842-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01)
Product NDC
67877-842
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220708
Marketing Category Name
ANDA
Application Number
ANDA215630
Manufacturer
Ascend Laboratories, LLC
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/67877-842-01