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"76420-713-01" National Drug Code (NDC)
Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (76420-713-01)
(Asclemed USA, Inc.)
NDC Code
76420-713-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (76420-713-01)
Product NDC
76420-713
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230823
Marketing Category Name
ANDA
Application Number
ANDA215630
Manufacturer
Asclemed USA, Inc.
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/76420-713-01