prednisone
Generic: prednisone
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
prednisone
Generic Name
prednisone
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
prednisone 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7686
Product ID
50090-7686_8fd53a70-cbae-427c-86d8-de10f36d9f6a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213385
Listing Expiration
2026-12-31
Marketing Start
2021-08-04
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907686
Hyphenated Format
50090-7686
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
ANDA213385 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-7686-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8fd53a70-cbae-427c-86d8-de10f36d9f6a", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312617"], "spl_set_id": ["6f326242-786c-44b5-9317-f5fb0485d8e2"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7686-6)", "package_ndc": "50090-7686-6", "marketing_start_date": "20251009"}], "brand_name": "prednisone", "product_id": "50090-7686_8fd53a70-cbae-427c-86d8-de10f36d9f6a", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-7686", "generic_name": "prednisone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA213385", "marketing_category": "ANDA", "marketing_start_date": "20210804", "listing_expiration_date": "20261231"}