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"72559-038-23" National Drug Code (NDC)
Famotidine 300 mg in 1 BOTTLE (72559-038-23)
(Little Pharma, Inc.)
NDC Code
72559-038-23
Package Description
300 mg in 1 BOTTLE (72559-038-23)
Product NDC
72559-038
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20250515
Marketing Category Name
ANDA
Application Number
ANDA215766
Manufacturer
Little Pharma, Inc.
Substance Name
FAMOTIDINE
Strength
10
Strength Unit
mg/10mg
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72559-038-23