pravastatin sodium
Generic: pravastatin sodium
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
pravastatin sodium
Generic Name
pravastatin sodium
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
pravastatin sodium 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4408
Product ID
70518-4408_3d315367-eb57-02f2-e063-6394a90a72c6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076056
Listing Expiration
2026-12-31
Marketing Start
2025-07-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184408
Hyphenated Format
70518-4408
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
- 20 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-4408-0)
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4408-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d315367-eb57-02f2-e063-6394a90a72c6", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["6cef5e92-26b7-435c-878f-72a05a624560"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4408-0)", "package_ndc": "70518-4408-0", "marketing_start_date": "20250728"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4408-1)", "package_ndc": "70518-4408-1", "marketing_start_date": "20250824"}], "brand_name": "Pravastatin sodium", "product_id": "70518-4408_3d315367-eb57-02f2-e063-6394a90a72c6", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4408", "generic_name": "Pravastatin sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_start_date": "20250728", "listing_expiration_date": "20261231"}