Package 60687-886-01

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 60687-886-01
Digits Only 6068788601
Product NDC 60687-886
Description

100 BLISTER PACK in 1 CARTON (60687-886-01) / 1 TABLET in 1 BLISTER PACK (60687-886-11)

Marketing

Marketing Status
Marketed Since 2025-03-02
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": "4600582d-4c2e-b8ce-e063-6394a90ace45", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475"], "spl_set_id": ["97f826f0-b5c5-410c-b1f0-523873981e8d"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-886-01)  / 1 TABLET in 1 BLISTER PACK (60687-886-11)", "package_ndc": "60687-886-01", "marketing_start_date": "20250302"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "60687-886_4600582d-4c2e-b8ce-e063-6394a90ace45", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "60687-886", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20250302", "listing_expiration_date": "20261231"}