Package 72162-1953-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 72162-1953-0
Digits Only 7216219530
Product NDC 72162-1953
Description

1000 TABLET in 1 BOTTLE (72162-1953-0)

Marketing

Marketing Status
Marketed Since 2024-03-11
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "72d78298-266a-45d6-9577-b4f3737134ab", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["51800012-406b-4389-817f-88dd21e338d1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1953-0)", "package_ndc": "72162-1953-0", "marketing_start_date": "20240311"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "72162-1953_72d78298-266a-45d6-9577-b4f3737134ab", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72162-1953", "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": "40 mg/1"}], "application_number": "ANDA209869", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}