prednisone
Generic: prednisone
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
66267-812
Product ID
66267-812_1fa78286-2610-a15e-e063-6294a90a1a53
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66267812
Hyphenated Format
66267-812
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (66267-812-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1fa78286-2610-a15e-e063-6294a90a1a53", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0366267812108"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["62ec965c-e682-9920-e053-2a91aa0adcdb"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66267-812-10)", "package_ndc": "66267-812-10", "marketing_start_date": "20180116"}], "brand_name": "Prednisone", "product_id": "66267-812_1fa78286-2610-a15e-e063-6294a90a1a53", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "66267-812", "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": "ANDA040362", "marketing_category": "ANDA", "marketing_start_date": "20010829", "listing_expiration_date": "20261231"}