pravastatin sodium

Generic: pravastatin sodium

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

Drug Facts

Product Profile

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

pravastatin sodium 80 mg/1

Manufacturer
Teva Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0480-7270
Product ID 0480-7270_95e8c960-5096-43a9-8807-89cdf404a214
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077793
Listing Expiration 2026-12-31
Marketing Start 2023-02-09

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 04807270
Hyphenated Format 0480-7270

Supplemental Identifiers

RxCUI
904481
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 ANDA077793 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (0480-7270-10)
  • 90 TABLET in 1 BOTTLE (0480-7270-98)
source: ndc

Packages (2)

0480-7270-10 1000 TABLET in 1 BOTTLE (0480-7270-10) 0480-7270-98 90 TABLET in 1 BOTTLE (0480-7270-98)

Ingredients (1)

pravastatin sodium (80 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": "95e8c960-5096-43a9-8807-89cdf404a214", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904481"], "spl_set_id": ["f66cb1c1-5ff1-4b0b-89d0-8ecaee26b0b8"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0480-7270-10)", "package_ndc": "0480-7270-10", "marketing_start_date": "20230320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0480-7270-98)", "package_ndc": "0480-7270-98", "marketing_start_date": "20230209"}], "brand_name": "Pravastatin Sodium", "product_id": "0480-7270_95e8c960-5096-43a9-8807-89cdf404a214", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0480-7270", "generic_name": "Pravastatin Sodium", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "ANDA077793", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}