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"63739-645-10" National Drug Code (NDC)
Famotidine 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-645-10) / 10 TABLET in 1 BLISTER PACK
(Mckesson Corporation DBA SKY Packaginng)
NDC Code
63739-645-10
Package Description
10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-645-10) / 10 TABLET in 1 BLISTER PACK
Product NDC
63739-645
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
Mckesson Corporation DBA SKY Packaginng
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/63739-645-10