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"64679-740-03" National Drug Code (NDC)
Ranitidine 10 BLISTER PACK in 1 CARTON (64679-740-03) > 10 TABLET, COATED in 1 BLISTER PACK
(Wockhardt USA LLC.)
NDC Code
64679-740-03
Package Description
10 BLISTER PACK in 1 CARTON (64679-740-03) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC
64679-740
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20080731
Marketing Category Name
ANDA
Application Number
ANDA078884
Manufacturer
Wockhardt USA LLC.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
75
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/64679-740-03