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"64679-374-07" National Drug Code (NDC)
Famotidine 10 BLISTER PACK in 1 CARTON (64679-374-07) > 10 TABLET in 1 BLISTER PACK
(Wockhardt USA LLC.)
NDC Code
64679-374-07
Package Description
10 BLISTER PACK in 1 CARTON (64679-374-07) > 10 TABLET in 1 BLISTER PACK
Product NDC
64679-374
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100806
Marketing Category Name
ANDA
Application Number
ANDA090837
Manufacturer
Wockhardt USA 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/64679-374-07