pravastatin sodium
Generic: pravastatin sodium
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
pravastatin sodium
Generic Name
pravastatin sodium
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
pravastatin sodium 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-4059
Product ID
68788-4059_f92e12bc-40c3-4afa-9190-2f4de11ec6b3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076056
Listing Expiration
2026-12-31
Marketing Start
2025-12-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687884059
Hyphenated Format
68788-4059
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
ANDA076056 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68788-4059-3)
- 60 TABLET in 1 BOTTLE (68788-4059-6)
- 90 TABLET in 1 BOTTLE (68788-4059-9)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f92e12bc-40c3-4afa-9190-2f4de11ec6b3", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458"], "spl_set_id": ["f92e12bc-40c3-4afa-9190-2f4de11ec6b3"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-4059-3)", "package_ndc": "68788-4059-3", "marketing_start_date": "20251208"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-4059-6)", "package_ndc": "68788-4059-6", "marketing_start_date": "20251208"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-4059-9)", "package_ndc": "68788-4059-9", "marketing_start_date": "20251208"}], "brand_name": "Pravastatin sodium", "product_id": "68788-4059_f92e12bc-40c3-4afa-9190-2f4de11ec6b3", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68788-4059", "generic_name": "Pravastatin sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_start_date": "20251208", "listing_expiration_date": "20261231"}