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"70518-3280-0" National Drug Code (NDC)

Chlorpromazine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3280-0)
(REMEDYREPACK INC.)

NDC Code70518-3280-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3280-0)
Product NDC70518-3280
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameChlorpromazine Hydrochloride
Non-Proprietary NameChlorpromazine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211201
Marketing Category NameANDA
Application NumberANDA212144
ManufacturerREMEDYREPACK INC.
Substance NameCHLORPROMAZINE HYDROCHLORIDE
Strength50
Strength Unitmg/1
Pharmacy ClassesPhenothiazine [EPC], Phenothiazines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3280-0





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