Package 42708-191-30

Brand: rosuvastatin calcium

Generic: rosuvastatin calcium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-191-30
Digits Only 4270819130
Product NDC 42708-191
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-191-30)

Marketing

Marketing Status
Marketed Since 2025-10-17
Brand rosuvastatin calcium
Generic rosuvastatin calcium
Sample Package Yes

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4148e517-edad-5cba-e063-6294a90a7a7f", "openfda": {"unii": ["83MVU38M7Q"], "rxcui": ["859747", "859751"], "spl_set_id": ["4148e0b3-0340-9f3a-e063-6394a90afc96"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-191-30)", "package_ndc": "42708-191-30", "marketing_start_date": "20251017"}], "brand_name": "Rosuvastatin calcium", "product_id": "42708-191_4148e517-edad-5cba-e063-6294a90a7a7f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42708-191", "generic_name": "Rosuvastatin calcium", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin calcium", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "20 mg/1"}], "application_number": "ANDA079172", "marketing_category": "ANDA", "marketing_start_date": "20160719", "listing_expiration_date": "20261231"}