Package 42708-108-30

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-108-30
Digits Only 4270810830
Product NDC 42708-108
Product ID 42708-108_459c810c-9310-6de5-e063-6394a90a48db
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-108-30)

Marketing

Marketing Status
Marketed Since 2018-04-26
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": "459c810c-9310-6de5-e063-6394a90a48db", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617311"], "spl_set_id": ["d8a72abf-1d43-47e1-88e8-c3c5cc4ba163"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-108-30)", "package_ndc": "42708-108-30", "marketing_start_date": "20180426"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "42708-108_459c810c-9310-6de5-e063-6394a90a48db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42708-108", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE", "strength": "40 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20120529", "listing_expiration_date": "20261231"}