Package 50090-7710-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7710-0
Digits Only 5009077100
Product NDC 50090-7710
Product ID 50090-7710_79939d2a-2217-4a82-beff-8276ed0c6847
Description

90 TABLET in 1 BOTTLE (50090-7710-0)

Marketing

Marketing Status
Marketed Since 2025-10-14
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "79939d2a-2217-4a82-beff-8276ed0c6847", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467"], "spl_set_id": ["45f0fd53-7160-4361-ba0b-3401095441c4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7710-0)", "package_ndc": "50090-7710-0", "marketing_start_date": "20251014"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50090-7710_79939d2a-2217-4a82-beff-8276ed0c6847", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7710", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}