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"0781-1719-10" National Drug Code (NDC)

Chlorpromazine Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1719-10)
(Sandoz Inc)

NDC Code0781-1719-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0781-1719-10)
Product NDC0781-1719
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameChlorpromazine Hydrochloride
Non-Proprietary NameChlorpromazine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19730103
Marketing Category NameANDA
Application NumberANDA080439
ManufacturerSandoz Inc
Substance NameCHLORPROMAZINE HYDROCHLORIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesPhenothiazine [EPC],Phenothiazines [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-1719-10





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