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"70934-017-20" National Drug Code (NDC)
Ranitidine 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-017-20)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)
NDC Code
70934-017-20
Package Description
20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-017-20)
Product NDC
70934-017
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine
Non-Proprietary Name
Ranitidine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20181025
Marketing Category Name
ANDA
Application Number
ANDA078542
Manufacturer
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance Name
RANITIDINE HYDROCHLORIDE
Strength
150
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/70934-017-20