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"72205-233-84" National Drug Code (NDC)
Famotidine 55 mL in 1 BOTTLE (72205-233-84)
(Novadoz Pharmaceuticals LLC)
NDC Code
72205-233-84
Package Description
55 mL in 1 BOTTLE (72205-233-84)
Product NDC
72205-233
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
POWDER, FOR SUSPENSION
Usage
ORAL
Start Marketing Date
20250724
Marketing Category Name
ANDA
Application Number
ANDA219863
Manufacturer
Novadoz Pharmaceuticals LLC
Substance Name
FAMOTIDINE
Strength
40
Strength Unit
mg/5mL
Pharmacy Classes
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72205-233-84