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"10202-194-51" National Drug Code (NDC)
7 Select Acid Controller 8 BLISTER PACK in 1 CARTON (10202-194-51) > 1 TABLET in 1 BLISTER PACK
(7-Eleven)
NDC Code
10202-194-51
Package Description
8 BLISTER PACK in 1 CARTON (10202-194-51) > 1 TABLET in 1 BLISTER PACK
Product NDC
10202-194
Product Type Name
HUMAN OTC DRUG
Proprietary Name
7 Select Acid Controller
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140805
End Marketing Date
20200131
Marketing Category Name
ANDA
Application Number
ANDA077351
Manufacturer
7-Eleven
Substance Name
FAMOTIDINE
Strength
20
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/10202-194-51