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"64679-742-03" National Drug Code (NDC)
Ranitidine 10 BLISTER PACK in 1 CARTON (64679-742-03) > 10 TABLET in 1 BLISTER PACK
(Wockhardt USA LLC.)
NDC Code
64679-742-03
Package Description
10 BLISTER PACK in 1 CARTON (64679-742-03) > 10 TABLET in 1 BLISTER PACK
Product NDC
64679-742
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20091211
Marketing Category Name
ANDA
Application Number
ANDA078701
Manufacturer
Wockhardt USA LLC.
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
300
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/64679-742-03