prednisone

Generic: prednisone

Labeler: cambridge therapeutics technologies, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler cambridge therapeutics technologies, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 5 mg/1

Manufacturer
Cambridge Therapeutics Technologies, LLC

Identifiers & Regulatory

Product NDC 70882-117
Product ID 70882-117_886eec2f-5b6d-4fce-bc0d-a10e445f041f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040362
Listing Expiration 2026-12-31
Marketing Start 2001-08-29

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 70882117
Hyphenated Format 70882-117

Supplemental Identifiers

RxCUI
312617
UPC
0370882117210 0370882117302
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 ANDA040362 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BLISTER PACK (70882-117-21)
  • 30 TABLET in 1 BLISTER PACK (70882-117-30)
source: ndc

Packages (2)

70882-117-21 21 TABLET in 1 BLISTER PACK (70882-117-21) 70882-117-30 30 TABLET in 1 BLISTER PACK (70882-117-30)

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": "886eec2f-5b6d-4fce-bc0d-a10e445f041f", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0370882117210", "0370882117302"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["d6246d5f-bf2b-4850-978e-6ea3148de095"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BLISTER PACK (70882-117-21)", "package_ndc": "70882-117-21", "marketing_start_date": "20010829"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70882-117-30)", "package_ndc": "70882-117-30", "marketing_start_date": "20010829"}], "brand_name": "Prednisone", "product_id": "70882-117_886eec2f-5b6d-4fce-bc0d-a10e445f041f", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70882-117", "generic_name": "Prednisone", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA040362", "marketing_category": "ANDA", "marketing_start_date": "20010829", "listing_expiration_date": "20261231"}