Package 42708-003-30

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-003-30
Digits Only 4270800330
Product NDC 42708-003
Product ID 42708-003_45b41a94-e930-c847-e063-6394a90ad348
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-003-30)

Marketing

Marketing Status
Marketed Since 2018-05-31
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": "45b41a94-e930-c847-e063-6394a90ad348", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310", "617311", "617312"], "spl_set_id": ["3e59aa97-5480-41e0-86b0-047e648b976d"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-003-30)", "package_ndc": "42708-003-30", "marketing_start_date": "20180531"}], "brand_name": "Atorvastatin Calcium", "product_id": "42708-003_45b41a94-e930-c847-e063-6394a90ad348", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42708-003", "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": "10 mg/1"}], "application_number": "ANDA205300", "marketing_category": "ANDA", "marketing_start_date": "20170504", "listing_expiration_date": "20261231"}