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"68084-172-01" National Drug Code (NDC)
Famotidine 100 BLISTER PACK in 1 CARTON (68084-172-01) > 1 TABLET in 1 BLISTER PACK (68084-172-11)
(American Health Packaging)
NDC Code
68084-172-01
Package Description
100 BLISTER PACK in 1 CARTON (68084-172-01) > 1 TABLET in 1 BLISTER PACK (68084-172-11)
Product NDC
68084-172
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20070320
End Marketing Date
20160131
Marketing Category Name
ANDA
Application Number
ANDA090837
Manufacturer
American Health Packaging
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/68084-172-01