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"70518-3083-0" National Drug Code (NDC)
Fluoxetine Hydrochloride 30 TABLET, COATED in 1 BLISTER PACK (70518-3083-0)
(REMEDYREPACK INC.)
NDC Code
70518-3083-0
Package Description
30 TABLET, COATED in 1 BLISTER PACK (70518-3083-0)
Product NDC
70518-3083
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Fluoxetine Hydrochloride
Non-Proprietary Name
Fluoxetine Hydrochloride
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20210504
Marketing Category Name
ANDA
Application Number
ANDA203836
Manufacturer
REMEDYREPACK INC.
Substance Name
FLUOXETINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3083-0