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"49999-237-30" National Drug Code (NDC)
Famotidine 30 TABLET in 1 BOTTLE (49999-237-30)
(Lake Erie Medical DBA Quality Care Products LLC)
NDC Code
49999-237-30
Package Description
30 TABLET in 1 BOTTLE (49999-237-30)
Product NDC
49999-237
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20010416
Marketing Category Name
ANDA
Application Number
ANDA075805
Manufacturer
Lake Erie Medical DBA Quality Care Products LLC
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/49999-237-30