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"80005-119-16" National Drug Code (NDC)
Famotidine 50 mL in 1 BOTTLE (80005-119-16)
(Carnegie Pharmaceuticals LLC)
NDC Code
80005-119-16
Package Description
50 mL in 1 BOTTLE (80005-119-16)
Product NDC
80005-119
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
POWDER, FOR SUSPENSION
Usage
ORAL
Start Marketing Date
20230810
Marketing Category Name
ANDA
Application Number
ANDA217137
Manufacturer
Carnegie 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/80005-119-16