pravastatin sodium

Generic: pravastatin sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-516
Product ID 71205-516_d1c530da-d15b-4ffc-b2b4-cd1e4dd5e8ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076341
Listing Expiration 2026-12-31
Marketing Start 2011-07-18

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 71205516
Hyphenated Format 71205-516

Supplemental Identifiers

RxCUI
904475
UPC
0371205516307
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 ANDA076341 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-516-30)
  • 60 TABLET in 1 BOTTLE (71205-516-60)
  • 90 TABLET in 1 BOTTLE (71205-516-90)
source: ndc

Packages (3)

71205-516-30 30 TABLET in 1 BOTTLE (71205-516-30) 71205-516-60 60 TABLET in 1 BOTTLE (71205-516-60) 71205-516-90 90 TABLET in 1 BOTTLE (71205-516-90)

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": "d1c530da-d15b-4ffc-b2b4-cd1e4dd5e8ee", "openfda": {"upc": ["0371205516307"], "unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["2bdfb0ef-2455-4ca2-a117-ce8e26bb2dbc"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-516-30)", "package_ndc": "71205-516-30", "marketing_start_date": "20201224"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-516-60)", "package_ndc": "71205-516-60", "marketing_start_date": "20201224"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-516-90)", "package_ndc": "71205-516-90", "marketing_start_date": "20201224"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "71205-516_d1c530da-d15b-4ffc-b2b4-cd1e4dd5e8ee", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71205-516", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}