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"0781-1883-10" National Drug Code (NDC)
Ranitidine Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1883-10)
(Sandoz Inc)
NDC Code
0781-1883-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (0781-1883-10)
Product NDC
0781-1883
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ranitidine Hydrochloride
Non-Proprietary Name
Ranitidine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19970829
Marketing Category Name
ANDA
Application Number
ANDA074467
Manufacturer
Sandoz Inc
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/0781-1883-10