Package 70771-1786-9

Brand: pitavastatin calcium

Generic: pitavastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70771-1786-9
Digits Only 7077117869
Product NDC 70771-1786
Description

90 TABLET in 1 BOTTLE (70771-1786-9)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e441676b-f28d-4506-9b0e-b8e28b1f7d1f", "openfda": {"unii": ["IYD54XEG3W"], "rxcui": ["861643", "861648", "861652"], "spl_set_id": ["7b1a9aa6-a7a4-4050-8a40-89ba9728555a"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1786-9)", "package_ndc": "70771-1786-9", "marketing_start_date": "20231102"}], "brand_name": "pitavastatin calcium", "product_id": "70771-1786_e441676b-f28d-4506-9b0e-b8e28b1f7d1f", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70771-1786", "generic_name": "pitavastatin calcium", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pitavastatin calcium", "active_ingredients": [{"name": "PITAVASTATIN CALCIUM", "strength": "4 mg/1"}], "application_number": "ANDA206047", "marketing_category": "ANDA", "marketing_start_date": "20231102", "listing_expiration_date": "20261231"}