0591-5052
Generic: prednisone
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
prednisone
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Active Ingredients
prednisone 5 mg/1
Identifiers & Regulatory
Product NDC
0591-5052
Product ID
0591-5052_d0862bb6-a3a3-459c-941c-1f4a7f93f1e1
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
1987-11-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915052
Hyphenated Format
0591-5052
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: label)
Generic Name
prednisone (source: ndc)
Application Number
ANDA080356 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 111000 TABLET in 1 BAG (0591-5052-00)
- 133332 TABLET in 1 CONTAINER (0591-5052-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "d0862bb6-a3a3-459c-941c-1f4a7f93f1e1", "openfda": {}, "finished": false, "packaging": [{"description": "111000 TABLET in 1 BAG (0591-5052-00)", "package_ndc": "0591-5052-00", "marketing_start_date": "01-NOV-87"}, {"description": "133332 TABLET in 1 CONTAINER (0591-5052-77)", "package_ndc": "0591-5052-77", "marketing_start_date": "30-JUN-24"}], "product_id": "0591-5052_d0862bb6-a3a3-459c-941c-1f4a7f93f1e1", "dosage_form": "TABLET", "product_ndc": "0591-5052", "generic_name": "Prednisone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "19871101", "listing_expiration_date": "20261231"}