pravastatin sodium

Generic: pravastatin sodium

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pravastatin sodium
Generic Name pravastatin sodium
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pravastatin sodium 40 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 61919-708
Product ID 61919-708_0e994ad4-d03f-9670-e063-6294a90adad3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207068
Listing Expiration 2026-12-31
Marketing Start 2019-01-15

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 61919708
Hyphenated Format 61919-708

Supplemental Identifiers

RxCUI
904467 904475
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 (61919-708-30)
source: ndc

Packages (1)

61919-708-30 30 TABLET in 1 BOTTLE (61919-708-30)

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": "0e994ad4-d03f-9670-e063-6294a90adad3", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467", "904475"], "spl_set_id": ["7f814fd9-7b35-67da-e053-2a91aa0a39dc"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (61919-708-30)", "package_ndc": "61919-708-30", "marketing_start_date": "20190115"}], "brand_name": "Pravastatin Sodium", "product_id": "61919-708_0e994ad4-d03f-9670-e063-6294a90adad3", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "61919-708", "generic_name": "Pravastatin Sodium", "labeler_name": "Direct_Rx", "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": "20190115", "listing_expiration_date": "20261231"}