Pravastatin Sodium

Generic: Pravastatin Sodium

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Pravastatin Sodium
Generic Name Pravastatin Sodium
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

PRAVASTATIN SODIUM 20 mg/1

Identifiers & Regulatory

Product NDC 70518-2887
Product ID 70518-2887_39e58968-532b-40ec-e063-6394a90a222a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076056
Marketing Start 2020-09-15
Marketing End 2026-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182887
Hyphenated Format 70518-2887

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1)
  • 30 TABLET in 1 BLISTER PACK (70518-2887-2)
source: ndc

Packages (2)

70518-2887-1 90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1) 70518-2887-2 30 TABLET in 1 BLISTER PACK (70518-2887-2)

Ingredients (1)

PRAVASTATIN SODIUM (20 mg/1)

Linked Drug Pages (1)

Pravastatin Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39e58968-532b-40ec-e063-6394a90a222a", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["0c4b59f1-92a8-44f8-8b4c-691f35777460"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1)", "package_ndc": "70518-2887-1", "marketing_end_date": "20260831", "marketing_start_date": "20220916"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2887-2)", "package_ndc": "70518-2887-2", "marketing_end_date": "20260831", "marketing_start_date": "20221108"}], "brand_name": "Pravastatin Sodium", "product_id": "70518-2887_39e58968-532b-40ec-e063-6394a90a222a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-2887", "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_end_date": "20260831", "marketing_start_date": "20200915"}