pravastatin sodium

Generic: pravastatin sodium

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pravastatin sodium 40 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-808
Product ID 43063-808_415b8e43-f5c7-10c5-e063-6394a90a9929
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207068
Listing Expiration 2026-12-31
Marketing Start 2017-12-11

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 43063808
Hyphenated Format 43063-808

Supplemental Identifiers

RxCUI
904475
UPC
0343063808306
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 ANDA207068 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-808-30)
source: ndc

Packages (1)

43063-808-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-808-30)

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": "415b8e43-f5c7-10c5-e063-6394a90a9929", "openfda": {"upc": ["0343063808306"], "unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["46fdf929-c961-4dd9-8865-8eb4adaa259a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-808-30)", "package_ndc": "43063-808-30", "marketing_start_date": "20171211"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "43063-808_415b8e43-f5c7-10c5-e063-6394a90a9929", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "43063-808", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA207068", "marketing_category": "ANDA", "marketing_start_date": "20171211", "listing_expiration_date": "20261231"}