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"72606-509-02" National Drug Code (NDC)
Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (72606-509-02)
(CELLTRION USA, INC.)
NDC Code
72606-509-02
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (72606-509-02)
Product NDC
72606-509
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200923
Marketing Category Name
ANDA
Application Number
ANDA075786
Manufacturer
CELLTRION USA, INC.
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/72606-509-02