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"70518-3590-0" National Drug Code (NDC)
Chlorpromazine Hydrochloride 30 TABLET, COATED in 1 BLISTER PACK (70518-3590-0)
(REMEDYREPACK INC.)
NDC Code
70518-3590-0
Package Description
30 TABLET, COATED in 1 BLISTER PACK (70518-3590-0)
Product NDC
70518-3590
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Chlorpromazine Hydrochloride
Non-Proprietary Name
Chlorpromazine Hydrochloride
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20221207
Marketing Category Name
ANDA
Application Number
ANDA212996
Manufacturer
REMEDYREPACK INC.
Substance Name
CHLORPROMAZINE HYDROCHLORIDE
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Phenothiazine [EPC], Phenothiazines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3590-0