0591-5321
Generic: primidone
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
primidone
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Active Ingredients
primidone 250 mg/1
Identifiers & Regulatory
Product NDC
0591-5321
Product ID
0591-5321_2cf67f61-1e32-42a2-8612-dd624bb4e239
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Listing Expiration
2026-12-31
Marketing Start
2010-06-19
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05915321
Hyphenated Format
0591-5321
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
primidone (source: label)
Generic Name
primidone (source: ndc)
Application Number
ANDA083551 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 27000 TABLET in 1 BAG (0591-5321-00)
- 32004 TABLET in 1 CONTAINER (0591-5321-77)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "2cf67f61-1e32-42a2-8612-dd624bb4e239", "openfda": {}, "finished": false, "packaging": [{"description": "27000 TABLET in 1 BAG (0591-5321-00)", "package_ndc": "0591-5321-00", "marketing_start_date": "19-JUN-10"}, {"description": "32004 TABLET in 1 CONTAINER (0591-5321-77)", "package_ndc": "0591-5321-77", "marketing_start_date": "07-AUG-24"}], "product_id": "0591-5321_2cf67f61-1e32-42a2-8612-dd624bb4e239", "dosage_form": "TABLET", "product_ndc": "0591-5321", "generic_name": "Primidone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "PRIMIDONE", "strength": "250 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_start_date": "20100619", "listing_expiration_date": "20261231"}