pravastatin sodium

Generic: pravastatin sodium

Labeler: safecor health llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler safecor health llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 40 mg/1

Manufacturer
Safecor Health LLC

Identifiers & Regulatory

Product NDC 48433-149
Product ID 48433-149_494d6f85-61ba-5c05-e063-6294a90a1dd3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076056
Marketing Start 2026-01-23
Marketing End 2026-09-30

Pharmacologic Class

Classes
hmg-coa reductase inhibitor [epc] hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 48433149
Hyphenated Format 48433-149

Supplemental Identifiers

RxCUI
904467 904475
UNII
3M8608UQ61

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
  • 40 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (48433-149-20) / 1 TABLET in 1 BLISTER PACK (48433-149-01)
source: ndc

Packages (1)

48433-149-20 100 BLISTER PACK in 1 CARTON (48433-149-20) / 1 TABLET in 1 BLISTER PACK (48433-149-01)

Ingredients (1)

pravastatin sodium (40 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": "494d6f85-61ba-5c05-e063-6294a90a1dd3", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467", "904475"], "spl_set_id": ["0ae196a4-be3d-4cd8-9ff2-68aeb91b8678"], "manufacturer_name": ["Safecor Health LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (48433-149-20)  / 1 TABLET in 1 BLISTER PACK (48433-149-01)", "package_ndc": "48433-149-20", "marketing_end_date": "20260930", "marketing_start_date": "20260123"}], "brand_name": "Pravastatin Sodium", "product_id": "48433-149_494d6f85-61ba-5c05-e063-6294a90a1dd3", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "48433-149", "generic_name": "Pravastatin Sodium", "labeler_name": "Safecor Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076056", "marketing_category": "ANDA", "marketing_end_date": "20260930", "marketing_start_date": "20260123"}