Package 68071-3895-9

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3895-9
Digits Only 6807138959
Product NDC 68071-3895
Product ID 68071-3895_422b2258-9fec-d426-e063-6294a90a620d
Description

90 TABLET in 1 BOTTLE (68071-3895-9)

Marketing

Marketing Status
Marketed Since 2025-09-16
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": "422b2258-9fec-d426-e063-6294a90a620d", "openfda": {"upc": ["0368071389593"], "unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["3ef390a6-e0a0-331d-e063-6394a90a83d0"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3895-9)", "package_ndc": "68071-3895-9", "marketing_start_date": "20250916"}], "brand_name": "Pravastatin sodium", "product_id": "68071-3895_422b2258-9fec-d426-e063-6294a90a620d", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3895", "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": "ANDA076056", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}