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"55111-396-16" National Drug Code (NDC)
Famotidine 5 BLISTER PACK in 1 CARTON (55111-396-16) / 5 TABLET in 1 BLISTER PACK
(Dr.Reddys Laboratories Limited)
NDC Code
55111-396-16
Package Description
5 BLISTER PACK in 1 CARTON (55111-396-16) / 5 TABLET in 1 BLISTER PACK
Product NDC
55111-396
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Famotidine
Non-Proprietary Name
Famotidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20060930
Marketing Category Name
ANDA
Application Number
ANDA077367
Manufacturer
Dr.Reddys Laboratories Limited
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/55111-396-16