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"70095-040-01" National Drug Code (NDC)
Deflazacort 1 BOTTLE in 1 CARTON (70095-040-01) / 100 TABLET in 1 BOTTLE
(Sun Pharmaceutical Industries Limited)
NDC Code
70095-040-01
Package Description
1 BOTTLE in 1 CARTON (70095-040-01) / 100 TABLET in 1 BOTTLE
Product NDC
70095-040
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Deflazacort
Non-Proprietary Name
Deflazacort
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20250319
Marketing Category Name
ANDA
Application Number
ANDA217741
Manufacturer
Sun Pharmaceutical Industries Limited
Substance Name
DEFLAZACORT
Strength
6
Strength Unit
mg/1
Pharmacy Classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70095-040-01