deflazacort

Generic: deflazacort

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name deflazacort
Generic Name deflazacort
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

deflazacort 30 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 70095-042
Product ID 70095-042_4583474c-40e7-dd9d-e063-6294a90a902a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217741
Listing Expiration 2026-12-31
Marketing Start 2025-03-19

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70095042
Hyphenated Format 70095-042

Supplemental Identifiers

RxCUI
153098 153880 1870954 1870958
UPC
0370095040015 0370095043306 0370095042309 0370095041302
UNII
KR5YZ6AE4B
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name deflazacort (source: ndc)
Generic Name deflazacort (source: ndc)
Application Number ANDA217741 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (70095-042-30) / 30 TABLET in 1 BOTTLE
source: ndc

Packages (1)

70095-042-30 1 BOTTLE in 1 CARTON (70095-042-30) / 30 TABLET in 1 BOTTLE

Ingredients (1)

deflazacort (30 mg/1)

Linked Drug Pages (1)

Deflazacort ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4583474c-40e7-dd9d-e063-6294a90a902a", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0370095040015", "0370095043306", "0370095042309", "0370095041302"], "unii": ["KR5YZ6AE4B"], "rxcui": ["153098", "153880", "1870954", "1870958"], "spl_set_id": ["fb5350d5-ead1-41f4-8b25-0da0bd7fcffe"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70095-042-30)  / 30 TABLET in 1 BOTTLE", "package_ndc": "70095-042-30", "marketing_start_date": "20250319"}], "brand_name": "Deflazacort", "product_id": "70095-042_4583474c-40e7-dd9d-e063-6294a90a902a", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70095-042", "generic_name": "Deflazacort", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deflazacort", "active_ingredients": [{"name": "DEFLAZACORT", "strength": "30 mg/1"}], "application_number": "ANDA217741", "marketing_category": "ANDA", "marketing_start_date": "20250319", "listing_expiration_date": "20261231"}