Prednisone

Generic: Prednisone

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Prednisone
Generic Name Prednisone
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

PREDNISONE 5 mg/1

Identifiers & Regulatory

Product NDC 70518-2486
Product ID 70518-2486_3dd105a5-3822-c40f-e063-6294a90a944f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040362
Marketing Start 2019-12-15
Marketing End 2026-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182486
Hyphenated Format 70518-2486

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 Prednisone (source: ndc)
Generic Name Prednisone (source: ndc)
Application Number ANDA040362 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-2486-3)
source: ndc

Packages (1)

70518-2486-3 30 TABLET in 1 BLISTER PACK (70518-2486-3)

Ingredients (1)

PREDNISONE (5 mg/1)

Linked Drug Pages (1)

Prednisone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3dd105a5-3822-c40f-e063-6294a90a944f", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["134cab29-18b5-4adb-bc8d-0fb82c20ce05"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2486-3)", "package_ndc": "70518-2486-3", "marketing_end_date": "20260501", "marketing_start_date": "20240704"}], "brand_name": "Prednisone", "product_id": "70518-2486_3dd105a5-3822-c40f-e063-6294a90a944f", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-2486", "generic_name": "Prednisone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA040362", "marketing_category": "ANDA", "marketing_end_date": "20260501", "marketing_start_date": "20191215"}