pravastatin sodium

Generic: pravastatin sodium

Labeler: dr.reddy's laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler dr.reddy's laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 20 mg/1

Manufacturer
Dr.Reddy's Laboratories Limited

Identifiers & Regulatory

Product NDC 55111-230
Product ID 55111-230_5f4e21ff-4bcc-df0d-a629-ba190d95edc0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076714
Listing Expiration 2026-12-31
Marketing Start 2009-12-31

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 55111230
Hyphenated Format 55111-230

Supplemental Identifiers

RxCUI
904458 904467 904475 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 ANDA076714 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (55111-230-01)
  • 500 TABLET in 1 BOTTLE (55111-230-05)
  • 30 TABLET in 1 BOTTLE (55111-230-30)
  • 90 TABLET in 1 BOTTLE (55111-230-90)
source: ndc

Packages (4)

55111-230-01 100 TABLET in 1 BOTTLE (55111-230-01) 55111-230-05 500 TABLET in 1 BOTTLE (55111-230-05) 55111-230-30 30 TABLET in 1 BOTTLE (55111-230-30) 55111-230-90 90 TABLET in 1 BOTTLE (55111-230-90)

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": "5f4e21ff-4bcc-df0d-a629-ba190d95edc0", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["99cc0546-bb2d-751e-edfd-1c15a1182e0c"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55111-230-01)", "package_ndc": "55111-230-01", "marketing_start_date": "20091231"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (55111-230-05)", "package_ndc": "55111-230-05", "marketing_start_date": "20091231"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (55111-230-30)", "package_ndc": "55111-230-30", "marketing_start_date": "20091231"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (55111-230-90)", "package_ndc": "55111-230-90", "marketing_start_date": "20091231"}], "brand_name": "Pravastatin sodium", "product_id": "55111-230_5f4e21ff-4bcc-df0d-a629-ba190d95edc0", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "55111-230", "generic_name": "Pravastatin sodium", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076714", "marketing_category": "ANDA", "marketing_start_date": "20091231", "listing_expiration_date": "20261231"}