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"70756-052-11" National Drug Code (NDC)
Famotidine 100 TABLET in 1 BOTTLE (70756-052-11)
(Lifestar Pharma LLC)
NDC Code
70756-052-11
Package Description
100 TABLET in 1 BOTTLE (70756-052-11)
Product NDC
70756-052
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20231019
Marketing Category Name
ANDA
Application Number
ANDA075302
Manufacturer
Lifestar Pharma LLC
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/70756-052-11