Package 71205-048-04

Brand: alendronate sodium

Generic: alendronate sodium
NDC Package

Package Facts

Identity

Package NDC 71205-048-04
Digits Only 7120504804
Product NDC 71205-048
Product ID 71205-048_6db7f218-1343-4b68-b72d-6605f1838e97
Description

1 BLISTER PACK in 1 CARTON (71205-048-04) / 4 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-06-01
Brand alendronate sodium
Generic alendronate sodium
Sample Package No

Linked Drug Pages (1)

Alendronate Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6db7f218-1343-4b68-b72d-6605f1838e97", "openfda": {"upc": ["0371205048044"], "unii": ["2UY4M2U3RA"], "rxcui": ["904431"], "spl_set_id": ["6c4d13fb-490c-4ea9-9b04-003c8d8e9f0c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-048-04)  / 4 TABLET in 1 BLISTER PACK", "package_ndc": "71205-048-04", "marketing_start_date": "20180601"}], "brand_name": "Alendronate Sodium", "product_id": "71205-048_6db7f218-1343-4b68-b72d-6605f1838e97", "dosage_form": "TABLET", "pharm_class": ["Bisphosphonate [EPC]", "Diphosphonates [CS]"], "product_ndc": "71205-048", "generic_name": "Alendronate Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alendronate Sodium", "active_ingredients": [{"name": "ALENDRONATE SODIUM", "strength": "70 mg/1"}], "application_number": "ANDA090124", "marketing_category": "ANDA", "marketing_start_date": "20080804", "listing_expiration_date": "20261231"}