Package 61919-708-30

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 61919-708-30
Digits Only 6191970830
Product NDC 61919-708
Product ID 61919-708_0e994ad4-d03f-9670-e063-6294a90adad3
Description

30 TABLET in 1 BOTTLE (61919-708-30)

Marketing

Marketing Status
Marketed Since 2019-01-15
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": "0e994ad4-d03f-9670-e063-6294a90adad3", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904467", "904475"], "spl_set_id": ["7f814fd9-7b35-67da-e053-2a91aa0a39dc"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (61919-708-30)", "package_ndc": "61919-708-30", "marketing_start_date": "20190115"}], "brand_name": "Pravastatin Sodium", "product_id": "61919-708_0e994ad4-d03f-9670-e063-6294a90adad3", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "61919-708", "generic_name": "Pravastatin Sodium", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA207068", "marketing_category": "ANDA", "marketing_start_date": "20190115", "listing_expiration_date": "20261231"}