pravastatin sodium

Generic: pravastatin sodium

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

Drug Facts

Product Profile

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

pravastatin sodium 20 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3361
Product ID 68071-3361_1ce9135a-5f51-1bdf-e063-6294a90a0164
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 680713361
Hyphenated Format 68071-3361

Supplemental Identifiers

RxCUI
904467
UPC
0368071336191
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
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3361-3)
  • 90 TABLET in 1 BOTTLE (68071-3361-9)
source: ndc

Packages (2)

68071-3361-3 30 TABLET in 1 BOTTLE (68071-3361-3) 68071-3361-9 90 TABLET in 1 BOTTLE (68071-3361-9)

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": "1ce9135a-5f51-1bdf-e063-6294a90a0164", "openfda": {"upc": ["0368071336191"], "unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["54228087-7ab0-5561-e054-00144ff8d46c"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3361-3)", "package_ndc": "68071-3361-3", "marketing_start_date": "20170712"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3361-9)", "package_ndc": "68071-3361-9", "marketing_start_date": "20170712"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "68071-3361_1ce9135a-5f51-1bdf-e063-6294a90a0164", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3361", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}