pravastatin sodium

Generic: pravastatin sodium

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 40 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-7202
Product ID 0093-7202_72579e23-23ef-4ab7-ad64-24d5ea7997eb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076056
Marketing Start 2006-04-25
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 00937202
Hyphenated Format 0093-7202

Supplemental Identifiers

RxCUI
904458 904467 904475
UPC
0300937202981
UNII
3M8608UQ61

Packaging Origin

Original Packager
true

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
  • 1000 TABLET in 1 BOTTLE (0093-7202-10)
  • 90 TABLET in 1 BOTTLE (0093-7202-98)
source: ndc

Packages (2)

0093-7202-10 1000 TABLET in 1 BOTTLE (0093-7202-10) 0093-7202-98 90 TABLET in 1 BOTTLE (0093-7202-98)

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": "72579e23-23ef-4ab7-ad64-24d5ea7997eb", "openfda": {"upc": ["0300937202981"], "unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475"], "spl_set_id": ["99e0e848-f8f3-4b42-b880-8fbc42633948"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0093-7202-10)", "package_ndc": "0093-7202-10", "marketing_end_date": "20260930", "marketing_start_date": "20060425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0093-7202-98)", "package_ndc": "0093-7202-98", "marketing_end_date": "20260930", "marketing_start_date": "20060425"}], "brand_name": "Pravastatin Sodium", "product_id": "0093-7202_72579e23-23ef-4ab7-ad64-24d5ea7997eb", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0093-7202", "generic_name": "Pravastatin Sodium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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": "20060425"}