prednisone
Generic: prednisone
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-020
Product ID
63187-020_df3fb8ca-6e08-4e2b-8e27-db94366273ab
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
63187020
Hyphenated Format
63187-020
Supplemental Identifiers
RxCUI
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
- 5 mg/1
Packaging
- 10 TABLET in 1 BOTTLE (63187-020-10)
- 15 TABLET in 1 BOTTLE (63187-020-15)
- 21 TABLET in 1 BOTTLE (63187-020-21)
- 30 TABLET in 1 BOTTLE (63187-020-30)
- 36 TABLET in 1 BOTTLE (63187-020-36)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "df3fb8ca-6e08-4e2b-8e27-db94366273ab", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["7c650dc8-43f6-4257-81ed-c93b00202d06"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (63187-020-10)", "package_ndc": "63187-020-10", "marketing_start_date": "20180904"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (63187-020-15)", "package_ndc": "63187-020-15", "marketing_start_date": "20180904"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (63187-020-21)", "package_ndc": "63187-020-21", "marketing_start_date": "20180904"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-020-30)", "package_ndc": "63187-020-30", "marketing_start_date": "20180904"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (63187-020-36)", "package_ndc": "63187-020-36", "marketing_start_date": "20180904"}], "brand_name": "Prednisone", "product_id": "63187-020_df3fb8ca-6e08-4e2b-8e27-db94366273ab", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "63187-020", "generic_name": "Prednisone", "labeler_name": "Proficient Rx LP", "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"}