Package 65862-635-90

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 65862-635-90
Digits Only 6586263590
Product NDC 65862-635
Product ID 65862-635_ec34b688-92eb-42c2-b417-c3aa7f0a0ece
Description

90 TABLET in 1 BOTTLE (65862-635-90)

Marketing

Marketing Status
Marketed Since 2017-02-02
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": "ec34b688-92eb-42c2-b417-c3aa7f0a0ece", "openfda": {"upc": ["0365862632906"], "unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["b06ed801-ddee-4f56-924a-59fcb451eae6"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-635-05)", "package_ndc": "65862-635-05", "marketing_start_date": "20170202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-635-90)", "package_ndc": "65862-635-90", "marketing_start_date": "20170202"}], "brand_name": "Pravastatin sodium", "product_id": "65862-635_ec34b688-92eb-42c2-b417-c3aa7f0a0ece", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "65862-635", "generic_name": "Pravastatin sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "ANDA203367", "marketing_category": "ANDA", "marketing_start_date": "20170202", "listing_expiration_date": "20261231"}