Package 71335-2687-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2687-1
Digits Only 7133526871
Product NDC 71335-2687
Description

90 TABLET in 1 BOTTLE (71335-2687-1)

Marketing

Marketing Status
Marketed Since 2025-06-26
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ab146e4d-067b-4cdc-b343-b72fa74b6f44", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["f074240e-ef6b-45f2-8c4d-cb5c0dbc81f1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2687-1)", "package_ndc": "71335-2687-1", "marketing_start_date": "20250626"}], "brand_name": "Pravastatin sodium", "product_id": "71335-2687_ab146e4d-067b-4cdc-b343-b72fa74b6f44", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71335-2687", "generic_name": "Pravastatin sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA209869", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}