pravastatin sodium

Generic: pravastatin sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7709
Product ID 50090-7709_f0d2cf93-5c22-4df7-b66a-0b90ce2a614b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077987
Listing Expiration 2026-12-31
Marketing Start 2024-06-01

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 500907709
Hyphenated Format 50090-7709

Supplemental Identifiers

RxCUI
904467
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 ANDA077987 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7709-0)
  • 90 TABLET in 1 BOTTLE (50090-7709-1)
source: ndc

Packages (2)

50090-7709-0 30 TABLET in 1 BOTTLE (50090-7709-0) 50090-7709-1 90 TABLET in 1 BOTTLE (50090-7709-1)

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": "f0d2cf93-5c22-4df7-b66a-0b90ce2a614b", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["635062df-9a84-4ff8-874c-dcee581a5555"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7709-0)", "package_ndc": "50090-7709-0", "marketing_start_date": "20251014"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7709-1)", "package_ndc": "50090-7709-1", "marketing_start_date": "20251014"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-7709_f0d2cf93-5c22-4df7-b66a-0b90ce2a614b", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7709", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}