pravastatin sodium
Generic: pravastatin sodium
Labeler: northwind health company, llcDrug Facts
Product Profile
Brand Name
pravastatin sodium
Generic Name
pravastatin sodium
Labeler
northwind health company, llc
Dosage Form
TABLET
Routes
Active Ingredients
pravastatin sodium 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82868-081
Product ID
82868-081_472074f5-7926-aa3d-e063-6394a90a011a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209869
Listing Expiration
2026-12-31
Marketing Start
2025-06-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82868081
Hyphenated Format
82868-081
Supplemental Identifiers
RxCUI
UNII
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
pravastatin sodium (source: ndc)
Generic Name
pravastatin sodium (source: ndc)
Application Number
ANDA209869 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (82868-081-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "472074f5-7926-aa3d-e063-6394a90a011a", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["47207487-0c6d-8da3-e063-6294a90a8aee"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-081-30)", "package_ndc": "82868-081-30", "marketing_start_date": "20250619"}], "brand_name": "Pravastatin sodium", "product_id": "82868-081_472074f5-7926-aa3d-e063-6394a90a011a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82868-081", "generic_name": "Pravastatin sodium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA209869", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}