Package 63629-8913-1

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 63629-8913-1
Digits Only 6362989131
Product NDC 63629-8913
Description

500 TABLET in 1 BOTTLE (63629-8913-1)

Marketing

Marketing Status
Marketed Since 2021-11-19
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": "337944c8-5831-8ba0-e063-6294a90a5989", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904481"], "spl_set_id": ["80ddec55-6a18-4b87-8a07-6ae86ad62853"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-8913-1)", "package_ndc": "63629-8913-1", "marketing_start_date": "20211119"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "63629-8913_337944c8-5831-8ba0-e063-6294a90a5989", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "63629-8913", "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": "80 mg/1"}], "application_number": "ANDA209869", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}