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"0781-1717-10" National Drug Code (NDC)
Chlorpromazine Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1717-10)
(Sandoz Inc)
NDC Code
0781-1717-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (0781-1717-10)
Product NDC
0781-1717
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Chlorpromazine Hydrochloride
Non-Proprietary Name
Chlorpromazine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19730103
Marketing Category Name
ANDA
Application Number
ANDA080439
Manufacturer
Sandoz Inc
Substance Name
CHLORPROMAZINE HYDROCHLORIDE
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-1717-10