Package 71335-2908-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2908-1
Digits Only 7133529081
Product NDC 71335-2908
Product ID 71335-2908_3e0f38e6-a515-4d76-9de4-34a83c38e8f2
Description

1000 TABLET in 1 BOTTLE (71335-2908-1)

Marketing

Marketing Status
Marketed Since 2025-10-30
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

PRAVASTATIN SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e0f38e6-a515-4d76-9de4-34a83c38e8f2", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["03e27551-b3bf-47dd-b3ec-cd9a66ace3c4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2908-1)", "package_ndc": "71335-2908-1", "marketing_start_date": "20251030"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "71335-2908_3e0f38e6-a515-4d76-9de4-34a83c38e8f2", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71335-2908", "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": "20 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20110718", "listing_expiration_date": "20261231"}