rosuvastatin

Generic: rosuvastatin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rosuvastatin
Generic Name rosuvastatin
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

rosuvastatin 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4296
Product ID 70518-4296_35bc2e4d-f1c6-438e-e063-6394a90aead0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206381
Listing Expiration 2026-12-31
Marketing Start 2025-02-26

Pharmacologic Class

Established (EPC)
hmg-coa reductase inhibitor [epc]
Mechanism of Action
hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184296
Hyphenated Format 70518-4296

Supplemental Identifiers

RxCUI
859751
UNII
413KH5ZJ73
NUI
N0000175589 N0000000121

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 rosuvastatin (source: ndc)
Generic Name rosuvastatin (source: ndc)
Application Number ANDA206381 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-0)
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-2)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4296-3)
source: ndc

Packages (4)

70518-4296-0 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-0) 70518-4296-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-1) 70518-4296-2 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-2) 70518-4296-3 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4296-3)

Ingredients (1)

rosuvastatin (20 mg/1)

Linked Drug Pages (1)

Rosuvastatin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35bc2e4d-f1c6-438e-e063-6394a90aead0", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["413KH5ZJ73"], "rxcui": ["859751"], "spl_set_id": ["ab8f6264-cf12-4523-92f1-2bd60b3da442"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-0)", "package_ndc": "70518-4296-0", "marketing_start_date": "20250226"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-1)", "package_ndc": "70518-4296-1", "marketing_start_date": "20250327"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4296-2)", "package_ndc": "70518-4296-2", "marketing_start_date": "20250407"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4296-3)", "package_ndc": "70518-4296-3", "marketing_start_date": "20250427"}], "brand_name": "Rosuvastatin", "product_id": "70518-4296_35bc2e4d-f1c6-438e-e063-6394a90aead0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4296", "generic_name": "Rosuvastatin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin", "active_ingredients": [{"name": "ROSUVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA206381", "marketing_category": "ANDA", "marketing_start_date": "20250226", "listing_expiration_date": "20261231"}