Package 0832-6050-90

Brand: pitavastatin

Generic: pitavastatin calcium
NDC Package

Package Facts

Identity

Package NDC 0832-6050-90
Digits Only 0832605090
Product NDC 0832-6050
Product ID 0832-6050_266944ba-7e94-48c6-e063-6394a90adc2e
Description

90 TABLET in 1 BOTTLE (0832-6050-90)

Marketing

Marketing Status
Marketed Since 2023-11-02
Brand pitavastatin
Generic pitavastatin calcium
Sample Package No

Linked Drug Pages (1)

Pitavastatin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "266944ba-7e94-48c6-e063-6394a90adc2e", "openfda": {"unii": ["IYD54XEG3W"], "rxcui": ["861643", "861648", "861652"], "spl_set_id": ["9ad1ecb9-822d-47c1-9f6f-6f771fa0f924"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (0832-6050-90)", "package_ndc": "0832-6050-90", "marketing_start_date": "20231102"}], "brand_name": "Pitavastatin", "product_id": "0832-6050_266944ba-7e94-48c6-e063-6394a90adc2e", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0832-6050", "generic_name": "Pitavastatin Calcium", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pitavastatin", "active_ingredients": [{"name": "PITAVASTATIN CALCIUM", "strength": "4 mg/1"}], "application_number": "ANDA205955", "marketing_category": "ANDA", "marketing_start_date": "20231102", "listing_expiration_date": "20261231"}