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"70095-041-30" National Drug Code (NDC)
Deflazacort 1 BOTTLE in 1 CARTON (70095-041-30) / 30 TABLET in 1 BOTTLE
(Sun Pharmaceutical Industries Limited)
NDC Code
70095-041-30
Package Description
1 BOTTLE in 1 CARTON (70095-041-30) / 30 TABLET in 1 BOTTLE
Product NDC
70095-041
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
18
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/70095-041-30