Package 42708-141-30

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-141-30
Digits Only 4270814130
Product NDC 42708-141
Product ID 42708-141_45869ffe-679c-db53-e063-6294a90a1f4a
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-141-30)

Marketing

Marketing Status
Marketed Since 2021-03-10
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package Yes

Linked Drug Pages (1)

Atorvastatin Calcium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45869ffe-679c-db53-e063-6294a90a1f4a", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["bd216f5d-f319-7d8d-e053-2a95a90aa9ce"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-141-30)", "package_ndc": "42708-141-30", "marketing_start_date": "20210310"}], "brand_name": "Atorvastatin Calcium", "product_id": "42708-141_45869ffe-679c-db53-e063-6294a90a1f4a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42708-141", "generic_name": "Atorvastatin Calcium", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA209288", "marketing_category": "ANDA", "marketing_start_date": "20181223", "listing_expiration_date": "20261231"}