prednisone

Generic: prednisone

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 10 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3746
Product ID 68071-3746_4a032fba-f907-4a13-e063-6294a90a2508
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215672
Listing Expiration 2027-12-31
Marketing Start 2022-03-28

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 680713746
Hyphenated Format 68071-3746

Supplemental Identifiers

RxCUI
198145
UPC
0368071374605
UNII
VB0R961HZT
NUI
N0000175576 N0000175450

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 ANDA215672 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (68071-3746-0)
  • 21 TABLET in 1 BOTTLE (68071-3746-1)
  • 20 TABLET in 1 BOTTLE (68071-3746-2)
  • 30 TABLET in 1 BOTTLE (68071-3746-3)
  • 15 TABLET in 1 BOTTLE (68071-3746-5)
source: ndc

Packages (5)

68071-3746-0 10 TABLET in 1 BOTTLE (68071-3746-0) 68071-3746-1 21 TABLET in 1 BOTTLE (68071-3746-1) 68071-3746-2 20 TABLET in 1 BOTTLE (68071-3746-2) 68071-3746-3 30 TABLET in 1 BOTTLE (68071-3746-3) 68071-3746-5 15 TABLET in 1 BOTTLE (68071-3746-5)

Ingredients (1)

prednisone (10 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": "4a032fba-f907-4a13-e063-6294a90a2508", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0368071374605"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["292e2529-711c-7b74-e063-6394a90a660d"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-3746-0)", "package_ndc": "68071-3746-0", "marketing_start_date": "20241213"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (68071-3746-1)", "package_ndc": "68071-3746-1", "marketing_start_date": "20251111"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3746-2)", "package_ndc": "68071-3746-2", "marketing_start_date": "20241213"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3746-3)", "package_ndc": "68071-3746-3", "marketing_start_date": "20260204"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68071-3746-5)", "package_ndc": "68071-3746-5", "marketing_start_date": "20241213"}], "brand_name": "PREDNISONE", "product_id": "68071-3746_4a032fba-f907-4a13-e063-6294a90a2508", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68071-3746", "generic_name": "PREDNISONE", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREDNISONE", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA215672", "marketing_category": "ANDA", "marketing_start_date": "20220328", "listing_expiration_date": "20271231"}